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Pella Recalls Sliding Patio Doors and Windows Over Button Battery Safety Concerns
Protect kids from button battery hazards with Pella's free repair offer
February 7, 2025A recall has been announced for select Pella sliding patio doors and windows with automated shades, as well as certain battery-operated remote controls. The U.S. Consumer Product Safety Commission (CPSC) issued this recall due to noncompliance with federal regulations for products containing button cell or coin batteries.
The batteries can be accessed by children, posing a risk of ingestion. Approximately 340 units are affected across the United States. The recall was prompted by federal safety checks that identified missing warning labels and the potential for children to remove the batteries.
Pella is removing affected units from distribution and contacting known purchasers to arrange free repairs or replacements.
What to look for?
Product Name and Description:
- Pella Reserve sliding doors with Insynctive technology (2-panel, 3-panel, and 4-panel)
- Pella Lifestyle sliding doors with Insynctive technology
- Pella Lifestyle windows with Insynctive remote control
- Battery-operated remote controls sold individually
- Some items display a Pella logo on the lower 1/3 of the remote; packaging may include Pella branding
Identifiers:
- Date codes on sliding doors: 031924 to 060524 (etched on the lower corner of the glass)
- Model numbers for window remote controls: 206A0000 (Generation 2) and 206A0001 (Generation 3)
- UPC code on packaging: 748171618722 for certain remote controls
- The lot or date code is typically found on the lower edge of the glass or on the remotes packaging
Affected purchase locations and dates:
- Distributed through Pella-authorized retailers and possibly online channels nationwide
- Sold in recent months leading up to the discovery of the regulatory violation
What should buyers do?
Immediate action:
- Remove any batteries from the door sensor housing and remote controls
- Keep the batteries in a place that children cannot reach
Refunds, replacements, or repairs:
- Contact Pella for complimentary remote replacement and free door repair by a qualified technician
- Call toll-free at 844-807-2219 or visit the companys website for details (MondayFriday, 8 AM5 PM ET)
Health and safety advice (if applicable):
- If someone, especially a child, may have swallowed a button cell battery, seek medical attention promptly
- Watch for symptoms such as coughing, wheezing, difficulty swallowing, or chest pain
Sources
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Doosan Bobcat Recalls 579 AirFX Mower Deck Attachments for Crush Hazard
Ensure Safety: Check Your AirFX Mower Deck for Faulty Locking Pins
February 7, 2025A voluntary recall has been issued by Doosan Bobcat North America for Bobcat & Steiner AirFX Finish Mower Deck attachments. The recall involves a crush hazard that occurs when the locking pins cannot be inserted to secure the mower deck in the upright or tilted position.
This issue was discovered following five reported incidents of unsuccessful attempts to install the locking pins; no injuries have been reported. Approximately 552 units were sold in the United States, and 27 were sold in Canada.
These products were distributed through authorized Bobcat dealers. The company is working with regulatory agencies to provide a free repair and is advising current owners to follow interim safety guidelines until the fix is available.
What to look for?
Product name and description:
- Bobcat & Steiner AirFX Finish Mower Deck attachments labeled with AirFX and either 72 or 61
- Black color and branded AirFX
- Used as attachments for lawn and ground maintenance
Identifiers:
- Model numbers: 7526575, 7526579, 7449223, 7447341
- The model number can typically be found on product labeling or the mower deck itself
Affected purchase locations and dates:
- Sold through authorized Bobcat dealerships in the United States and Canada
- The attachments were sold before the recall announcement date (check purchase or service records to confirm)
What should buyers do?
Immediate actions:
- If the locking pins cannot be inserted while the deck is in the upright or tilted position, discontinue regular use of that maintenance position
- Use two straps, each rated for 1,500 lbs., to secure the deck when performing service or maintenance until a repair is completed
Refunds, replacements, or repairs:
- A free repair will be provided
- Contact customer support at 800-743-4340, Monday through Friday, 9 AM - 5 PM CT, or visit the website listed below to request service or learn more
- If shipping is needed, request a prepaid return label from customer support
Health and safety advice:
- Do not attempt to force the locking pins into place
- If an injury occurs during deck adjustment or service, seek medical attention promptly
Sources
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Pearhead Recalls Infant Learning Sets Due to Choking Hazard from Wooden Rattle; Over 2,700 Units Affected in US and Canada
Pearhead recalls learning sets; wooden rattle poses choking risk
February 7, 2025A recall has been issued for Pearhead Learning Sets, model number 87150. This action was taken in conjunction with the U.S. Consumer Product Safety Commission due to a potential choking hazard associated with the wooden egg-shaped rattle in the set.
The rattle can become lodged in a child's throat and does not meet federal safety standards for infant rattles. According to reports, approximately 2,700 units are affected in the United States, with an additional 288 in Canada.
These items were distributed through various retail and online outlets. The company has removed the products from the marketplace and is working with authorities to address consumer concerns. No injuries have been reported at this time.
What to look for?
- Product name and description:
- Pearhead Learning Sets, labeled for babies 0-6 months
- Includes eight pieces (cow stroller toy, crinkle sheep toy, black and white tummy time book with flashcards, plush activity cube, wooden egg shaker rattle, and others)
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Packaged in a box marked learning set developmental toys for babies 0-6 months
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Identifiers:
- Model number: 87150
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The model number may appear on a label on the box or on accompanying documentation
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Affected purchase locations & dates:
- Sold through multiple retailers and online in the United States and Canada
- Distributed throughout 2023 (specific sales dates may vary by retailer)
What should buyers do?
- Next steps:
- Immediately stop using the egg-shaped rattle
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Contact the manufacturer for guidance, replacement, or refund
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Refunds, replacements, or repairs:
- Reach customer support at 888-308-4928 (toll-free), MondayFriday, 9:30 AM6 PM ET
- Email service@pearhead.com to request assistance
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Visit the manufacturers recall page to initiate a prepaid return
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Health & safety advice:
- If a child has used the rattle and experienced any difficulty breathing or coughing, seek medical attention
Sources
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Ariens Recalls Over 6,000 Sno-Thro Snow Throwers Due to Laceration Hazard
Ariens Snow Throwers Recalled: Free Repairs for Rotating Part Hazard
February 7, 2025Ariens Company has announced a voluntary recall of certain DELUXE-, PLATINUM-, and PROFESSIONAL-series Sno-Thro snow throwers due to a laceration hazard linked to the impeller and auger assembly continuing to rotate after the control lever is released.
The recall, issued on February 6, 2025, was conducted in cooperation with the U.S. Consumer Product Safety Commission. It affects approximately 6,264 units in the United States and 108 units in Canada. No injuries have been reported to date.
The recalled units were sold through authorized Ariens dealers in the United States and Canada from August 2024 to September 2024. Ariens Company is arranging free repairs and has taken steps to address the issue.
What to look for?
Product name and description:
- Ariens DELUXE-, PLATINUM-, and PROFESSIONAL-series Sno-Thro snow throwers
- Bright orange exterior with rear wheels or tracks
Identifiers:
- Model and serial numbers are located on the white square ID tag on the frame
Affected purchase locations and dates:
- Sold at authorized Ariens dealers throughout the United States and Canada
- Available from August 2024 to September 2024
What should buyers do?
Product handling:
- Stop using the recalled snow throwers immediately
- Contact the manufacturer or an authorized dealer to arrange for a free repair
Refunds, replacements, or repairs:
- Buyers are eligible for a free repair
- Contact Ariens Company at 877-740-7060 (Monday through Friday, 8 AM to 4 PM CT) or visit the website listed below for further assistance
Health and safety advice:
- The recalled units pose a laceration risk from rotating parts
- Anyone who experiences an injury should contact a healthcare provider for further evaluation
Sources
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Half million LG oven ranges recalled after starting fires
Federal regulators have received 28 reports of fires
February 6, 2025Appliance maker LG recalled around 500,000 slide-in and freestanding electric ranges following more than two dozen reported fires and hundreds of thousands of dollars in property damage.
The company said the front-mounted knobs on the recalled ranges can be accidentally switched onby humans or pets.
The U.S. Consumer Product Safety Commission has received at least 86 reports of unintentional activation of the front-mounted knobs. These LG ranges have been involved in more than 28 fires. At least five fires caused extensive property damage totaling over $340,000. At least eight minor injuries have been reported, including burns, and there have been reports of three fires involving pet deaths.
The ranges were sold at Best Buy, Costco, The Home Depot, Lowes, and other appliance stores nationwide and online at LG.com. Depending upon the model, the ranges were sold from 2015 through January 2025 for between $1,400 and $2,650.
"LG is reminding consumers about our unique safety function called Lock Out or Control Lock available on LG electric ranges with front-mounted knobs since 2015," the company said in a statement to ConsumerAffairs.
"In cooperation with the CPSC, LG will provide a more prominent label that reminds consumers to use the exclusive Control Lock/Lock Out function. When activated, this innovative function, available only on LG ranges, locks the cooktop heating elements from being turned on even when the knob is turned."
What to do
Consumers should contact LG to get a warning label and placement instructions.The label reminds owners to use the Lock Out/Control Lock function on the range control panel to disable activation of the heating elements when the range is not in use.
LG said to view the instructions regarding the control lock/lock out feature on a video hosted on Vimeo.
Consumers are cautioned to keep children and pets away from the knobs, to check the range knobs to ensure they are off before leaving home or going to bed, and not to leave objects on the range when the range is not in use.
Consumers may contact LG at 800-399-3265 from 9 a.m. to 6 p.m. ET Monday through Friday, email at lgrange.recall@lge.com, or at LG's website lgecares.com/rangerecall and enter your information to request a free warning sticker, instructions on where to place the sticker, and how to use the Control Lock or Lock Out feature on their range.
Consumers may contact LG at 800-399-3265 from 9 a.m. to 6 p.m. ET Monday through Friday, email at lgrange.recall@lge.com, or at https://lgecares.com/rangerecall and enter your information to request a free warning sticker, instructions on where to place the sticker, and how to use the Control Lock or Lock Out feature on their range.
Email Mark Huffmanat mhuffman@consumeraffairs.com.
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Training cycles recalled due to fall hazard
The company has received reports of the seat unexpectedly lowering
February 6, 2025Johnson Health Tech North America has issued a recall for 12,885 Matrix training cycles due to a fall hazard. The training cycles adjustable seat can unexpectedly lower while in use, posing a fall hazard to the rider.
The firm has received 63 reports of seats unexpectedly lowering, including two reports that users fell off the cycle when the seat lowered. No injuries have been reported.
This recall involves certain Matrix-brand Training Cycles models CXP-03, CXC-02, CXM-03, CXV and CXM-02. The recalled products have adjustable saddles and handlebars with an aluminum rear flywheel and a magnetic resistance system.
They have matte black steel frames, forged steel cranks, dual-sided SPD pedals, four leveling feet and two transport wheels. Matrix is printed on the side. The model and serial numbers are located on a label on the lower rear area of the cycle frame. Recalled cycles have a serial number that contains a serial prefix of FC32, ZFC32B, FC33, FC36, FC29D or FC27.
The products were sold primarily to commercial fitness facilities, both by JHTNA directly and through third-party distributors, from January 2021 through October 2024 for between $2,530 and $7,305.
What to do
Consumers should immediately stop using the recalled cycles and contact Johnson Health Tech North America Inc. to schedule a service technician to install a free repair kit.
Consumers may contact Johnson Health Tech North America Inc. (JHTNA) toll-free at 866-218-3674 from 8 a.m. to 5 p.m. CT, Monday through Friday, email at cxrecall@matrixfitness.com or online at https://www.matrixfitness.com/us/eng/recalls, or go to www.matrixfitness.com and click on Recalls for more information. The firm is contacting all known purchasers directly.
Email Mark Huffman at mhuffman@consumeraffairs.com
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Alvogen recalls Fentanyl Transdermal System 25 patches
Some patches may stick together, delivering unhealthy amounts of the drug
February 5, 2025Alvogen has issued a nationwide recall of one lot of Fentanyl Transdermal System 25 patches because the patches may stick together, providing unhealthy even fatal - dosages.
The company says there is a possibility that the application of a multi-stacked 25 mcg/h patch could result in serious, life-threatening, or fatal respiratory depression. Groups at potentially increased risk could include first-time recipients of such patches, children, and the elderly. So far, Alvogen has received one serious adverse event related to this recall.
The product is used for the management of severe and persistent pain in opioid-tolerant patients who require an extended treatment period with a daily opioid analgesic. The affected Fentanyl Transdermal System lot is:
Lot 108319 of Fentanyl Transdermal System, 25 mcg/h, expiration date 04/2027.
This lot of Fentanyl Transdermal System was distributed nationwide at the pharmacy and patient level.
What to do
Alvogen, Inc. is notifying its distributors and direct customers by certified letter and is arranging for the return and replacement of all recalled products. Pharmacies are requested not to dispense any product subject to this recall
Patients who have the product subject to this recall should immediately remove any patch currently in use and contact their healthcare provider. Patients with any unused product should return it to the point of purchase for replacement. Consumers should contact their physician or health care provider if they have experienced any problems that may be related to taking or using this drug product.
Questions regarding this recall should be directed to Alvogen Customer Complaints by calling 866-770-3024 or sending an e-mail to alvogensmb@continuumindia.com, Monday to Friday from 9:00 am to 5:00 pm EST.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
Email Mark Huffman at mhuffman@consumeraffairs.com
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Cozchique Tebbis and Beeziac girls' pajamas recalled for fire risk
The clothing was sold exclusively on Amazon
February 4, 2025About 6,000 Cozchique Tebbis and Beeziac girls pajamas are being recalled because the pajama sets violate federal flammability regulations for childrens sleepwear, posing a risk of burn injuries to children.
Online at Amazon.com from May 2024 through September 2024 for between $12 and 17. No incidents have been reported.
This recall involves styles of Cozchique, Tebbis and Beeziac girls pajama sets. They are sold in sizes 4T, 5T, 6, 8, 10, 12, 14. The two-piece shirt and shorts sets came in six prints, including Tebbis "Sleepy Panda"; Cozchique "Pink & Gray Sloth", "Stripe Easter Bunny", and "Cherry"; and Beezizac "Panda & Donut" and "Blue Avocado."
The label on the shorts lists the size, fabric content 65% cotton 35% polyester, washing instructions and Made in China. The second sewn in labels has the batch ID, manufacture date and location. Impacted units have the batch number 20240415TTL, 20240501TTL or 20240509TTL. Cozchique, Tebbis or Beeziac is printed on the pajamas hang tags.
What to do
Consumers should immediately take the recalled pajamas away from children, stop using them, and contact Tupop to receive a full refund. Consumers should destroy the garments by cutting the top and bottom in half and dispose of them.
Consumers should send the recalling firm a photo of the destroyed garments by email at bzzservice@hotmail.com to receive a full refund. Tupop and Amazon are contacting all known purchasers directly.
Consumers may contact Tupop by email at bzzservice@hotmail.com for more information.
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Gerber recalls and discontinues some teething sticks
The company has received reports of choking incidents
February 3, 2025Gerber Products Company is initiating a recall and discontinuation of all batches of Gerber Soothe N Chew Teething Sticks due to a potential choking hazard for babies and young children.
Gerber Soothe N Chew Teething Sticks were distributed nationwide via the internet and to distribution centers and retail stores in 44 states and Puerto Rico.
Recalled products can be identified as follows:
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GERBER SOOTHE N CHEW TEETHING STICKS STRAWBERRY APPLE, Net Wt. 3.2 Oz (90g), with UPC 0 15000 04618 7, all lot codes
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GERBER SOOTHE N CHEW TEETHING STICKS BANANA, Net Wt. 3.2 Oz (90g), with UPC 0 15000 04608 8, all lot codes
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GERBER SOOTHE N CHEW TEETHING STICKS BANANA, Net Wt. 1.59 Oz (45g), with UPC 0 15000 01015 7, all lot codes
This recall and discontinuation is isolated to Gerber Soothe N Chew Teething Sticks strawberry apple and Gerber Soothe N Chew Teething Sticks banana.
The recall was initiated after receiving consumer complaints of choking incidents. To date, one emergency room visit has been reported to the firm.
What to do
Consumers who may have purchasedGerber Soothe N Chew Teething Sticks should not feed this product to their child and can return the product to the retailer where it was purchased for a refund. Anyone concerned about an injury or illness should contact a healthcare provider. For any additional support needed, Gerber is available 24/7 at 1-800-4-GERBER (1-800-443-7237).
We are working with the U.S. Food & Drug Administration (FDA) on this recall and will cooperate with them fully, the company said in a statement.
We sincerely apologize for any concern or inconvenience this action represents to parents, caregivers and retail customers.
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Dark chocolate pretzels recalled over milk allergen
The pretzels sold online in Connecticut, New Jersey and New York
January 31, 2025United Natural Trading has voluntarily recalled dark-chocolate-coveredpretzelsbecause they can cause an undeclared milk allergy, the company said Thursday.
Individuals with milk allergies or sensitivities mayexperience severe allergic reactions if they consume the recalled product.
No illnesses have been reported.
Recall details
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Product: Fresh Direct Dark Chocolate Covered Pretzels
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Reason for recall: Undeclared milk allergen
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Lot number: 24353
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Best by date: 06/30/2025
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Universal productcode: 811102026276
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Distribution: Limited quantities sold online to Connecticut, New Jerseyand New York
What should buyers do?
Consumers who purchased the recalled pretzels should:
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Avoid consuming the product if they have a milk allergy.
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Discard any remaining product.
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Keep proof of purchase (receipts or packaging) to request a refund.
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Contact United Natural Trading LLC at 732-650-9905 (Monday Friday, 9:00 am to 5:00 pm EST) with any questions.
Email Dieter Holger at dholger@consumeraffairs.com.
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Stadium seats recalled after two reports of falls and one injury
The Consumer Product Safety Commission says the security hook can break
January 31, 2025AMX Global is recalling 22,500 folding stadium seats due to fall and injury hazards. The company has received five reports of the security hook breaking, including two reports of falls and one injury involving bruising, headaches and a pinched nerve.
This recall involves the AMX Global Portable Folding Stadium Seat sold under the BJs Wholesale or Black Sierra brand. The BJs units have the Berkley Jensen logo on the back top side. The Black Sierra units have a Black Sierra Equipment logo on the top, right front side.
The stadium seats fold down to a compact size of about 4 inches by 20 inches by 19 inches from the open size of 16 inches by 20 inches by 19 inches. They have a padded handle and shoulder strap. Recalled Berkley Jensen seats have the date code 04/2022 on the white tag on the bottom of the seat. Recalled Black Sierra Equipment seats have the date codes 05/2022 or 11/2022 on the white tag on the bottom of the seat. Only those date codes are included in this recall.
The seats were sold at BJs Wholesale Club and Big 5 Corp stores nationwide and online at Amazon.com from July 2022 through January 2024 for between $30 and $50.
What to do
Consumers should immediately stop using the recalled seats. Consumers are directed to destroy the recalled seat by cutting through the fabric of the seat and backrest. Consumers are further directed to take a photo of the destroyed recalled seat, including the consumers initials and the date in the photo, and send the photo to AMX Global at support@stadiumseatrecall.com to receive a full refund.
Consumers may contact AMX Global toll-free at 888-439-5139 from 9 a.m. to 4:30 p.m. ET Monday through Friday, or email at support@stadiumseatrecall.com or online at https://stadiumseatrecall.com/or go to www.amxglobalinc.com and click on RECALL INFORMATION at the top of the page for more information.
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Refillable medicine bottles recalled because they aren’t child-proof enough
The plastic lids closure can degrade after repeated openings
January 31, 2025Cabinet Health has issued a recall for its four-ounce refillable medicine bottles because they lack proper child resistance. The Consumer Product Safety Commission says that poses a risk of child poisoning.
According to regulators, the plastic lids closure can degrade after repeated openings, causing the lids child-resistance to diminish, posing a risk of poisoning if the contents are swallowed by young children.
This recall involves certain Cabinet Health 4 oz. Refillable Medicine Bottles with ABS plastic lids. The bottles are made of clear glass with blue, turquoise, orange or purple plastic lids labeled CABINET. Cabinet Health sold the bottles filled with over-the-counter drugs or as empty 4 oz. bottles. The recalled empty 4 oz. bottles were sold via cabinethealth.com from March 2023 through July 2024.
Consumers with recalled empty bottles can identify them by the date of purchase. The recalled bottles filled with over-the-counter drugs have the following date codes on a sticker on the bottom of the bottle.
The products were sold online at cabinethealth.com, Amazon.com and Grove.co and at CVS stores from March 2023 through July 2024 for between $10 and $20.
What to do
Consumers should immediately secure the recalled bottles out of the sight and reach of children and contact Cabinet Health for a free replacement lid. Consumers will be asked to submit a photo demonstrating the destruction of the recalled lid. Cabinet Health and Amazon are contacting all known purchasers directly. This recall does not affect the medication within the bottles.
Consumers may contact Cabinet Health collect at 908-242-6108 from 9 a.m. to 5 p.m. ET Monday through Friday, email at recall@wearecabinet.com, or online at https://cabinethealth.com/voluntaryrecall or https://cabinethealth.com and click Recall at the bottom of the page for more information.
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Drug used to treat low blood pressure recalled
The drug may contain foreign matter
January 27, 2025Provepharm is recalling lot number 24020027; Expiry Date December 2025 of Phenylephrine hydrochloride Injection, USP, 10 mg/ mL at the hospital/institutional level. This recall was initiated based on a customer complaint to a pharmacy after observing a visible black particulate matter found in a single-sealed vial of the product.
Administration of an injectable product containing particulate matter may cause local irritation or swelling as a response to the foreign material. If the particulate matter enters the blood vessels, it can travel to various organs and potentially blocking blood vessels in the heart, lungs or brain, leading to serious complications such as stroke or even death.
So far, the company has not received any reports of adverse events or injuries associated with this recall.
Phenylephrine hydrochloride Injection is used for the treatment of clinically important hypotension resulting primarily from vasodilation in the setting of anesthesia and is packaged in 10 mL vial, 1 single dose vial, with NDC code as 81284-213-01.
The product can be identified by product name on carton and vial label and with lot number 24020027 and Exp. Date: Dec 2025 (NDC 81284-213-01). Phenylephrine hydrochloride Injection, USP, 10 mg/ mL, was distributed nationwide in the United States to wholesalers.
What to do
Provepharm Inc., in collaboration with its recall provider, Sedgwick, is notifying distributors and customers via UPS Ground and coordinating the return of all recalled products.
Wholesalers, distributors, compounding companies and hospitals in procession of the recalled Phenylephrine hydrochloride Injection, USP, 10 mg/ mL lot number 24020027, Exp date December 2025, should immediately cease use of and return the product to Sedgwick at the following address:
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Sedgwick
Event## 8664
2670 Executive Drive, Suite A
Indianapolis, IN 46241
Customers with questions regarding this recall can contact from 8:00 am to 5:00 pm (EST) Monday - Friday at:
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Product Returns:
Contact Sedgwick at:
IVR: 866-737-5394
FAX: 866-250-4503
Email: provepharm8664@sedgwick.com -
Medical-related Questions Contact Medical Information at:
1-833-727-6556
Email: safety-us@provepharm.com
Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.
Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online, by regular mail or by fax.
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First Aid Beauty recalls nearly 3,000 jars of popular moisturizer
The company said the jars were not intended for distribution
January 24, 2025First Aid Beauty has issued a recall for 2,756 14-ounce jars of its Ultra Repair Cream, colloidal oatmeal 0.5% Coconut Vanilla. According to the U.S. Food and Drug Administration enforcement notice, the jars were intended for quarantine but were inadvertently distributed.
The company explained on its website:
On November 20, 2024, First Aid Beauty discovered that we inadvertently sold 14 oz Ultra Repair Cream Coconut Vanilla on our direct-to-consumer site, FirstAidBeauty.com. This product was not intended for market sale.
We are recalling the Ultra Repair Cream Coconut Vanilla that were sold only on FirstAidBeauty.com in the United States. We issued an email directly to impacted consumers, proactively sent a replacement Ultra Repair Cream Grapefruit, and provided direction to stop product use of the Ultra Repair Cream Coconut Vanilla and discard.
If you did not receive an email from us regarding the product recall, then there is no additional action needed at this time. With questions or concerns, consumers can contact customerservice@firstaidbeauty.com or 800-322-3619.
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Veyer recalls 64,000 office chairs due to a fall hazard
The bolts securing the back may fail
January 21, 2025Veyer has issued a recall for 64,000 WorkPro office chairs because the bolts that connect the back of the chair to its base can fail, posing a fall hazard to users.
Veyer has received seven reports of consumers falling out of the chair, resulting in two minor injuries. The chairs were sold at Office Depot and OfficeMax stores nationwide and online at www.amazon.com, www.officedepot.com, www.walmart.com, www.ebay.com and other websites from October 2021 through September 2024 for about $430.
This recall involves WorkPro Momentum office chairs. The recalled ergonomic chairs were sold in black (model number 8517865) or gray (model number 2864384) and have a metal frame, cushioned seat, five coaster wheels and a high back that shifts side-to-side. The model number is located underneath the seat cushion.
What to do
Consumers should immediately stop using the recalled chair until repaired, and contact Veyer to receive a free repair kit, including shipping, and installation instructions. The repair kit consists of a back bracket, three bolts, an Allen wrench and a decorative cover. Veyer is contacting all known purchasers directly.
Consumers may contact Veyer toll-free at 833-881-0087 from 8:30 a.m. to 5 p.m. CT Monday through Friday, email at support@momentumwarranty.com, or online at https://help.officedepot.com/app/answers/detail/a_id/7555/kw/recall or www.officedepot.com/ and click on Recall Notices at the bottom of the page for more information.
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Space heaters recalled due to shock hazard
The Vornado Air heaters were sold on Amazon.com
January 17, 2025Vornado Air is recalling nearly 8,000 whole room heaters due to electric shock and fire hazards. The heaters were sold exclusively online at Amazon.com from August 2024 through October 2024 for about $90.
The recall involves Vornado VH2 Whole Room Heaters with a JUL24 or AUG24 date code and TYPE VH2 printed on the silver rating label on the underside of the heater.
The heaters are off-white and have thermostatic temperature control, automatic or continuous fan operation and two heat settings. Vornado with a red V behind it is printed on the front of the unit. Only units with a JUL24 or AUG24 date code are included in this recall.
What to do
Consumers should immediately stop using the recalled heaters and contact Vornado to confirm that their product is part of the recall and receive instructions on how to receive a free replacement heater.
Consumers may contact Vornado toll-free at 844-205-7978 from 8 a.m. to 5 p.m. CT Monday through Friday, email at vh2recall@vornado.com or online at www.vornado.com/recalls/vh2 or www.vornado.com and click on Product Recalls at the top of the webpage to check if your heater is included in the recall.
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Lexmark recalls printers after fire
Lexmark is offering a repair part
January 16, 2025Lexmark is recalling around 43,510 printers after reports of overheating and a fire, the Consumer Product Safety Commission said Thursday.
What are the product details?
- Product name:Lexmark specialty printers
- Model numbers: MS725dvn and MX725adve
Where were they sold?
Between $1,000 and $4,200, the printers sold at Lexmark.com, CDW Logistics, Tech Data Product Management Inc. and Insight Direct USA from June 2018through Nov. 2024, the CPSC said.
What should buyers do?
Owners of the printers should immediately stop using the printersand contact Lexmark for a free repair part, which snaps into the unit inside the rear-access panel, the CPSC said.
Lexmark can be reached by phone at +1-866-470-1574and by email atsafety@lexmark.com.
Image of Lexmark'sMX725adve printer. Image via CPSC.
Have there been any incidents?
There have been two reports of the printers overheating and one fire, but no injuries or damage, the CPSC said.
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Swivel shop stools recalled because the seat may break off from its post
Northern Tool + Equipment has received 18 reports of injuries from falls
January 16, 2025Northern Tool + Equipment is recalling nearly 52,000 adjustable swivel shop stools with backrests because of a fall hazard. The welded connection point between the seat base and the stool post can break, the company said.
The company has received reports of 271 incidents related to the recalled stools, including 18 reports of injuries from falls, and 20 reports of falls without injury.
Northern Tool + Equipment stores nationwide and online at NorthernTool.com, Walmart.com, Amazon.com and Ebay.com from September 2020 through June 2023 for about $80.
This recall involves Northern Tool + Equipment Adjustable Swivel Shop Stools with Backrests. The NT logo is on the seat of the recalled shop stool. Model No. 20230 and Intradin Co., Ltd. are printed on separate labels located underneath the stools seat. Only stools manufactured by Intradin Co. Ltd. are included in this recall.
What to do
Consumers should immediately stop using the recalled stools and contact Northern Tool + Equipment to receive a free replacement stool by completing the form at https://www.northerntool.com/recall-details-20230. The stool should be disposed of in accordance with any local and state laws.
Consumers may contact Northern Tool + Equipment toll-free at 888-518-0342 from 8 a.m. to 5 p.m. CT Monday through Friday, email Northern Tool + Equipment at inquiry@northerntool.com, visit online at https://www.northerntool.com/recall-details-20230 or www.northerntool.com and click on Product Recalls on the bottom of the homepage, or visit a Northern Tool + Equipment store for more information.
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Thousands of smoke alarms recalled due to failure to detect fires
The units were sold exclusively by HSN
January 16, 2025Three61hass issued a recall for about 328,000 Samurai smoke alarms because they may fail to warn owners of a fire. The units were sold exclusively by HSN.
Smoke sensitivity tests performed on the alarms by CPSC found that one of the detectors that was tested failed to alert when exposed to pre-determined concentrations of smoke.
This recall involves Samurai-branded mini smoke alarms, model number SM1. The white and silver plastic smoke alarms measure about 2.5 by 2.5 by 2.5 inches. They were sold in packs of two or three alarms and came with lithium-ion batteries, adhesive stickers, screws, mounting plates and an instruction manual.
Smoke appears on the front of the alarm below a button and installed on on the back. The model number is located on the product packaging. Three61 has received eight reports of the alarms failing to activate in the presence of smoke. No injuries have been reported.
What to do
Consumers should immediately contact Three61 for a free replacement alarm, including shipping. To register, consumers must write Recalled with a permanent marker on the smoke alarm and submit a photo of the marked product to the recall website at www.samuraibrands.com/recall.
Once registered, the firm will immediately ship the replacement alarm. Consumers should keep the recalled smoke alarms installed until receiving the replacement alarm. Consumers should install the replacement alarms immediately upon receiving them. Three61 is contacting all known purchasers directly.
Consumers may contact Three61 via email at recall@samuraibrands.com, or online at www.samuraibrands.com/recall or www.samuraibrands.com and click the recall banner on the top of the page for more information.
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Taquitos sold at ALDI recalled after metal injures buyer
Regulators worry the taquitos are lying in freezers
January 13, 2025Bestway Sandwiches is recalling 24,870 pounds of itsCasa Mamita frozen taquitos sold at ALDI after they contained metal that causeda dental injury, the U.S. Department of Agriculturesaid Saturday.
What are the product details?
- Product name:Casa Mamita Chicken & Cheese Taquitos
- Best by dates:07/03/25 and 09/25/25
- Size:20-ounce cartons
Where were they sold?
The frozen taquitos sold at ALDI grocery stores nationwide, the USDA said.
What should buyers do?
The frozen taquitos should be thrown away or returned to the place of purchase, the USDA said.
The USDA said it "is concerned that some product may be in consumers freezers."
Have there been any injuries?
One buyer reportedly suffered a dental injury, the USDA said.
Another buyer complained that a piece of metal was found in the food.