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Consumer Affairs Recalls - Products, Vehicles, Foods

  1. The nationwide recall includes more than 207,000 pounds of meat

    By Mark Huffman of ConsumerAffairs
    July 26, 2024

    PhotoBoar's Head Provisions Co. is recalling all liverwurst products currently on the market because it may be contaminated with Listeria monocytogenes.

    The U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) also announced that the company is recalling additional deli meat products that were produced on the same line and on the same day as the liverwurst and, therefore, may be tainted as well. The company is recalling approximately 207,528 pounds of products.

    The ready-to-eat liverwurst products were produced between June 11, 2024, and July 17, 2024, and have a 44-day shelf life. The following liverwurst products are subject to recall:

    • 3.5-lb. loaves in plastic casing, or various weight packages sliced in retail delis, containing Boars Head Strassburger Brand Liverwurst MADE IN VIRGINIA. The products shipped to retailers bear sell by dates ranging July 25, 2024, to Aug. 30, 2024, printed on the side of the packaging.

    The other ready-to-eat deli meat products were produced on June 27, 2024. The following deli meat products are subject to recall:

    • 9.5-lb. and 4.5-lb. full product, or various weight packages sliced in retail delis, containing Boars Head VIRGINIA HAM OLD FASHIONED HAM with sell by date AUG 10 on the product packaging.

    • 4-lb., or various weight packages sliced in retail delis, containing Boars Head ITALIAN CAPPY STYLE HAM with sell by date AUG 10 on the product packaging.

    • 6-lb., or various weight packages sliced in retail delis, containing Boars Head EXTRA HOT ITALIAN CAPPY STYLE HAM with sell by date AUG 10 on the product packaging.

    • 4-lb., or various weight packages sliced in retail delis, containing Boars Head BOLOGNA with sell by date AUG 10 on the product packaging.

    • 2.5-lb., or various weight packages sliced in retail delis, containing Boars Head BEEF SALAMI with sell by date AUG 10 on the product packaging.

    • 5.5-lb., or various weight packages sliced in retail delis, containing Boars Head STEAKHOUSE ROASTED BACON HEAT & EAT with sell by date AUG 15 on the product packaging.

    • 3-lb., or various weight packages sliced in retail delis, containing Boars Head GARLIC BOLOGNA with sell by date AUG 10 on the product packaging.

    • 3-lb., or various weight packages sliced in retail delis, containing Boars Head BEEF BOLOGNA with sell by date AUG 10 on the product packaging.

    Distributed nationwide

    The products subject to recall were distributed to retail deli locations nationwide. The products shipped to deli retailers bear establishment number EST. 12612 inside the USDA mark of inspection on the product labels.

    The problem was discovered when FSIS was notified that a sample collected by the Maryland Department of Health tested positive for L. monocytogenes. The Maryland Department of Health, in collaboration with the Baltimore City Health Department, collected an unopened liverwurst product from a retail store for testing as part of an outbreak investigation of L. monocytogenes infections.

    Further testing is ongoing to determine if the product sample is related to the outbreak. Anyone concerned about illness should contact a healthcare provider.

    FSIS is working with the Centers for Disease Control and Prevention (CDC) and state public health partners to investigate the multistate outbreak of L. monocytogenes infections linked to meats sliced at delis.

    Severe illnesses reported

    As of July 25, 2024, 34 sick people have been identified in 13 states, including 33 hospitalizations and two deaths. Samples were collected from sick people from May 29, 2024, to July 12, 2024.

    Additional information may be found on the CDC investigation notice, Listeria Outbreak Linked to Meats Sliced at Delis. The recall is a Class I, the most urgent, and the investigation is ongoing.

    What to do

    FSIS is concerned that some product may be in consumers refrigerators and in retail deli cases. Consumers who have purchased these products are urged not to consume them and retailers are urged not to sell these products with the referenced sell by dates.

    These products should be thrown away or returned to the place of purchase. Consumers who have purchased these products are also urged to clean refrigerators thoroughly to prevent the risk of cross-contamination.

    Consumers with questions regarding the recall can contact Boars Head Provisions Co., Inc., Customer Service at 1-800-352-6277. Media with questions can contact Elizabeth Ward, vice president of Communications, Boars Head Provisions Co., Inc., at media@boarshead.com.

    Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers who need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

  2. This is the 63rd recall involving Kawasaki

    By Dieter Holger of ConsumerAffairs
    July 26, 2024

    PhotoKawasaki is recalling around 19,100 of its 2024 Kawasaki Mule PRO 1000 Off-Highway Utility Vehicles because a fire can ignite when the engine starts up, adding to a long list of recalls by the company due to fire hazards.

    There have been reports of three fires but no injuries, the Consumer Product Safety Commission said TuesdayThis is the 63rd recall involving Kawasaki products and 24thdue to a fire or burn hazard since 1981, according to a search of the CPSC's database.

    Kawasaki dealers nationwide sold seven models of thevehicles for$15,100 to$21,900 betweenJune 2023 through April 2024. The vehicles were made in the United States.

    See a table below on which models of the Kawasaki vehicles are recalled.

    What to do

    Owners should stop using the utility vehicles and contact a Kawasaki dealer to schedule a free repair. Kawasaki is directly contacting known buyers.

  3. So far, no illnesses have been reported

    By Mark Huffman of ConsumerAffairs
    July 25, 2024

    PhotoWeirs Farm has expanded its July 12 recall of whole and bagged cucumbers to include more produce in more stores in more states. The company said the recalled produce could be contaminated with Listeria monocytogenes.

    The expansion is in response to an investigation by Ohio health officials. Products involved in this expanded recall were packed between July 5-12.

    The company points out there have been no illnesses or consumer complaints reported to date and the recall is being carried out out of an abundance of caution.

    The recalled produce was sold at select Walmart stores in CT, DE, IL, IN, KY, MD, MI, NJ, NY, OH, PA, VA, and WV. The products include:

    • Wiers Farm Bagged Poblano - UPC 073064202581 16 oz bag

    • Wiers Farm Bagged Cubanelle - UPC 073064201836 16 oz bag

    • Wiers Farm Bagged Green Beans UPC 073064200846 variable weight bag

    • Wiers Farm Bagged Salad Cucumber UPC 073064459619 2 lb. bag

    • Wiers Farm Bagged Serrano UPC 073064201829 4 oz bag

    • Wiers Farm Organic Bell Pepper UPC 073064201416 2 count tray

    • Wiers Farm Organic Cucumber UPC 073064201423 2 count tray

    • Wiers Farm Organic Yellow Squash UPC 073064201447 2 count tray

    • Wiers Farm Organic Zucchini Squash UPC 073064201430 2 count tray

    Some Aldi stores are now included

    The following recalled produce products were sold at Aldi stores in KY, NY, OH, PA and WV:

    • Freshire Farms Bagged Green Beans 16 oz bag

    • Freshire Farms Bagged Jalapenos 8 oz bag

    In addition, these bulk items were sold individually or by the pound and are also included in the recall:

    • Anaheim peppers

    • Cilantro sold in bunches

    • Cubanelle peppers

    • Cucumber whole

    • Green beans

    • Green Bell Pepper

    • Habanero peppers

    • Hungarian Wax peppers

    • Jalapeno peppers

    • Mixed Vegetable Box (shipped to Cleveland and Youngstown, Ohio Foodbanks only)

    • Mustard Greens sold in bunches

    • Pickling Cucumber

    • Plain Parsley sold in bunches

    • Poblano peppers

    • Serrano peppers

    • Tomatillos

    Those produce items were sold at Kroger, Walmart and Save-A-Lot in various states.

    What to do

    Consumers should discard any suspect products. The product involved is past its shelf life and should already be out of distribution, but if consumers have any product they question, do not consume it, but rather discard it.

    For any questions or concerns, consumers may contact us at (419) 933-2161 or email us at customercare@wiersfarm.com.

  4. The recall covers vehicles manufactured over a five-year period

    By Mark Huffman of ConsumerAffairs
    July 24, 2024

    PhotoBMW has issued a recall for 291,112 vehicles for a recently discovered safety issue. The National Highway Transportation Administration (NHTSA) says that if the vehicles were rear-ended in a crash, the interior cargo rails could come loose, increasing the risk of an injury.

    Certain X3 sDrive30i, X3 xDrive30i, X3 M40i, and X3 M vehicles, manufactured between 2018 and 2023 are covered by the recall.

    What to do

    According to NHTSA, dealers will replace the rear cargo rail attachment bolts the source of the problem at no charge.

    To learn if your vehicle is included in the recall, go to NHTSAs recall website and enter your license plate number or 17-digit VIN.

    Earlier this month, BMW recalled nearly 400,000 vehicles because a defect could cause an airbag to explode.

  5. The recall includes 2019 to 2021 models

    By Mark Huffman of ConsumerAffairs
    July 23, 2024

    PhotoChrysler has issued a recall for 3,600 2019 to 2021 Pacifica plug-in hybrid vehicles because of a fire hazard. The company warns that the battery pack may cause a vehicle fire when parked, even with the ignition in the "Off" position.

    The company said the problem appears to be in the hybrid propulsion system.

    What to do

    Owners are advised not to charge their vehicles, and to park outside and away from structures, until they are repaired. To find out if you vehicle is included in the recall, go to the National Highway Transportation Administrations recall web site and enter the vehicles license plate number or 17-digit VIN.

    Dealers will update the high voltage battery pack control module (BPCM) software. In addition, dealers will inspect and if necessary, replace the battery pack assembly.

    Repairs will be performed free of charge. Owner notification letters are expected to be mailed by September 6, 2024. Owners may contact FCA US LLC customer service at 1-800-853-1403. FCA US LLC's number for this recall is 72B. This recall is an expansion of NHTSA recall number 22V-077.

    Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.nhtsa.gov.

  6. The FDA warns they contain acetaminophen, diclofenac and phenylbutazone

    By Mark Huffman of ConsumerAffairs
    July 23, 2024

    PhotoGURU Inc. is recalling Infla-650 Herbal Dietary Supplement Capsules, Lot No. IN-032, 700 mg to the consumer/user level.

    The U.S. Food and Drug Administration (FDA) reports Infla-650 capsules has been found to be tainted withacetaminophen, diclofenac and phenylbutazone, which are not listed on the label. Products containing acetaminophen, diclofenac and phenylbutazone cannot be marketed as dietary supplements.

    Infla-650 Herbal Dietary Supplement Capsules is an unapproved new drug for which safety and efficacy have not been established and, therefore, subject to recall.

    The FDA warns that use of the product poses a serious threat to consumers because it may result in unintentional acetaminophen overdose, especially if it is used in combination with other acetaminophen-containing products.

    Acetaminophen overdose can cause liver damage (hepatoxicity), ranging in severity from abnormalities in liver function to acute liver failure, and even death. People who experience unintentional acetaminophen overdose may not seek prompt medical attention because the symptoms of liver damage can take several days to emerge, even in severe cases.

    GURU Inc. has not received any reports of adverse events to date related to this recall.

    The tainted product is marketed as an herbal dietary supplement for pain relief and is packaged in stand-up pouches of 60 capsules. The affected Infla-650 product, include the following Lot No. IN-032 and expiration date: NOV. 2027. The product can be identified by silver standup pouch with green in white color theme label.

    What to do

    GURU Inc. is notifying its distributors and customers by email and is arranging for the return of all recalled products. Consumers and retailers that have Infla-650 which is being recalled should stop using/return to the place of purchase.

    Consumers with questions regarding this recall can contact GURU Inc. at (470) 536 9800 or info@nutraherbusa.com Monday to Friday, 9:00 AM to 5:00 PM Eastern Time (ET). Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product.

  7. NHTSA says a fuel pump failure could result in loss of drive power

    By Mark Huffman of ConsumerAffairs
    July 22, 2024

    PhotoHyundai has issued a recall for as many as 54,647 vehicles because their fuel pumps could fail, resulting in a loss of drive power.

    According to the National Highway Traffic Safety Administration (NHTSA), the recall covers some 2019 through 2023 models of the Genesis G70, Veloster N, Elantra N, and Kona N.

    The agency explained that the fuel pumps in question could experience premature wearing in the fuel control valve, allowing excess fuel to enter the fuel pump and the air and fuel mixture can result in a reduction or loss of motive power at low speeds, increasing the risk of a crash."

    What to do

    Owners of affected vehicles should receive a notification letter by mid-September. Dealers will install an updated fuel control valve plunger design and revise engine ECM software logic.

    In the meantime, NHTSA says owners should watch for "MIL illumination, lack of power, rough idle or misfire," as signs of trouble. To learn if a particular vehicle is included in the recall, go to the NHTSA recall page and enter the vehicles 17-digit VIN or license plate number.

  8. The manufacturer has issued a Stop Ride notice to consumers

    By Mark Huffman of ConsumerAffairs
    July 19, 2024

    PhotoCFMOTO has issued a recall for 3,630 FORCE 950 recreational off-highway vehicles (ROVs) due to a crash and tip-over hazard.

    The company said the shock absorber rod assembly can unthread and detach, causing the suspension to collapse and increase the risk of a crash.

    This recall involves 2022-2023 CFMOTO ZFORCE 950 HO Sport Side-by-Side Recreational Off Highway Vehicles sold in gray, orange, and tan colors. CFMOTO is stamped on the front of the vehicle and ZFORCE is printed on the side of the chassis. The VIN is stamped on the vehicles frame, just ahead of the right rear wheel.

    CFMOTO Powersports has received approximately 86 reports of incidents in which the shock absorber failed and the suspension collapsed, including one tip-over which resulted in impact injury to the ribs. The vehicles were sold at CFMOTO dealers nationwide from March 2022 through June 2024 for about $14,000.

    What to do

    Consumers should immediately stop using the recalled ROVs, and contact an authorized CFMOTO dealer to schedule an appointment to bring the recalled vehicle into the dealer for a free repair.

    CFMOTO has issued a Stop Ride notice to consumers and is contacting all registered owners and dealers directly to provide more details about the repair.

    Consumers may contact CFMOTO toll-free 888-823-6686 from 8 a.m. to 5 p.m. CT, Monday through Friday, email at info@cfmotousa.com, or online at https://www.cfmotousa.com/vehicle-recall or www.cfmotousa.com and go to Vehicle Recall under the Customer Care column for more information.

  9. The agency has raised the recall to Class II

    By Mark Huffman of ConsumerAffairs
    July 19, 2024

    PhotoWehah Farms has recalled 4,600 cases of Lundberg Family Farms Sustainable Wild Blend Gourmet Rice and the U.S. Food and Drug Administration (FDA) has raised the threat level to Class II, second most severe.

    The bags of rice may "contain foreign object that appears to be of rodent origin." The bags of rice were distributed in Arizona, California, Florida, Maine, New Hampshire, Oregon, and Wisconsin.

    The FDA did not say what rodent parts were found to be in the product, nor did it suggest how they got there.

    The recalled products are packaged in 1lb bags and bear the lot code 231004, with a best before date of October 4, 2024.

    What to do

    Consumers who have purchased the recalled products should not consume them but discard them or return them to the store where they were purchased for a refund.

  10. The hand-held steam cleaners pose a burn hazard

    By Mark Huffman of ConsumerAffairs
    July 18, 2024

    PhotoBISSELL is recalling 3.2 million Steam Shot handheld steam cleaners because they can expel hot water or steam onto users while heating or during use, posing a burn hazard.

    This recall involves multiple models of the BISSELL Steam Shot Handheld Steam Cleaners in the model series 39N7 and 2994. STEAM SHOT or POWER STEAMER is printed on the side of the product.

    The model numbers are printed on the product rating label located on the bottom of the unit. Colors include green, pink, blue, orange, white, black, purple and red.

    BISSELL has received 183 reports of hot water or steam escaping from the product, including 157 reports of minor burn injuries. The products were sold at Target, Walmart, and other department and home goods stores nationwide, and online at www.bissell.com, www.amazon.com, www.hsn.com, and other websites from August 2008 through May 2024 for between $35 and $40, or $70 for a two-pack.

    What to do

    Consumers should immediately stop using the recalled steam cleaners, and contact BISSELL to receive either a $60 credit to be used towards a BISSELL.com purchase, or a $40 refund for each of the recalled steam cleaners.

    Consumers should visit www.BISSELL.com/steamshotrecall to register for the recall, and for instructions on how to cut the cord and take and upload a photo of the steam cleaner showing the model number and cut cord.

    Consumers may also Contact BISSELL toll-free at 855-417-7001 from 9 a.m. to 9 p.m. ET Monday through Friday and 9 a.m. to 8 p.m. ET on Saturday, email RecallNA@bissell.com, or online at www.BISSELL.com/steamshotrecall or www.BISSELL.com and click on Product Recalls for more information.

  11. Routine testing uncovered Listeria monocytogenes

    By Mark Huffman of ConsumerAffairs
    July 17, 2024

    PhotoWiers Farm Inc. of Willard, Ohio, is recalling a limited number of whole cucumbers with a pack date of June 5, 2024 and bagged salad cucumbers with a pack date of June 5, 2024 and June 6, 2024. The producer says they could be contaminated with Listeria monocytogenes.

    The products were distributed in Walmart stores in Michigan, Ohio and Indiana. The potential contamination was discovered by the Michigan Department of Agriculture and Rural Development (MDARD) through routine sampling.

    There have been no illnesses or consumer complaints reported to date.

    Product Details

    Product Name: Whole Cucumbers

    Size: 1.5-2.5 inch diameter, 6-9 inch length

    Product Name: Wiers Farm 2 lb bagged Salad Cucumber

    Packaging: clear bag with blue base

    What to do

    Consumers should discard the products. The product involved is past its shelf life and should already be out of distribution, but if consumers have any product they question, do not consume it, but rather discard it. For any questions or concerns, consumers may contact the distributor at (419) 933-2161 or email at customercare@wiersfarm.com.

  12. Its the firms second medical device recall this month

    By Mark Huffman of ConsumerAffairs
    July 17, 2024

    PhotoBaxter International Inc., is recalling another medical device, the second recall in July. The company this week announced an Urgent Medical Device Recall for certain lots of the Volara system single-patient use circuit and blue ventilator adapter assembly.

    The recall is due to reports of the handset plug disconnecting from the nebulizer port on the blue ventilator adapter. To date, there have been no injuries reported in association with this issue. Baxter is working with customers to replace the affected products.

    When using the Volara system in-line with a ventilator and without a nebulizer connected to the blue ventilator adapter, the handset plug is required to help ensure proper operation and ventilator gas flow. If the handset plug disconnects and goes unnoticed prior to or during therapy, it may lead to an interruption or delay of care. This may result in reduced ventilation and oxygenation due to the ventilator leaking gas flow from the nebulizer port on the blue ventilator adapter.

    What to do

    Baxter has contacted affected customers, instructing them to stop using the affected patient circuits and arrange for the return and replacement of the accessories by contacting Baxter directly. If a patient does not have another option for therapy, they may continue to use it with caution. Customers are instructed to visually inspect the nebulizer port prior to therapy and check for any ventilator gas flow leaks for the duration of therapy.

    The Urgent Medical Device Recall applies to the Volara system single-patient use circuit with product codes M08473 and M08474, and the blue ventilator adapter assembly, product code M07937. The impacted accessories were distributed in the United States between Aug. 26, 2022 and Dec. 30, 2023.

    Consumers may contact Baxter Advanced Respiratory customer service at 800-426-4224 between the hours of 8 a.m. and 5 p.m. Central Time, Monday through Friday. Select option 2 for Acute Care Customer Service or option 3 for Home Care Customer Service.

    Reporting to the FDA MedWatch Serious Injury Reporting Program:

    Online: By completing and submitting the report online at: https://www.accessdata.fda.gov/scripts/medwatch/

    Regular mail or fax: Download the form from www.fda.gov/MedWatch/getforms.htm or call 800-332-1088 to request a reporting form, then complete and mail it to the address on the pre-addressed form, or submit by fax to 800-332-0178.

  13. The products were mostly distributed to food service operations

    By Mark Huffman of ConsumerAffairs
    July 16, 2024

    PhotoAW Farms is recalling approximately 6,900 pounds of hot dog products that were produced without the benefit of federal inspection.

    The U.S. Department of Agricultures Food Safety and Inspection Service (FSIS) said the ready-to-eat hot dogs were produced on various dates since approximately May 30, 2024, and have a shelf-life of 45 days. The following products are subject to recall:

    • 10-lb. boxes containing two 5-lb. vacuum-packed packages containing FRENCH CITY FOODS 6 12-1 HOTDOGS and PACKED ON with various dates since approximately May 30, 2024, represented on the label.

    • 10-lb. boxes containing two 5-lb. vacuum-packed packages containing frozen PORK, BEEF, DEXTROSE, SALT, SUGAR MAPLE GEO BROWN ALL MEAT HOTDOGS and PACKED ON with various dates since approximately May 30, 2024, represented on the label.

    • 10-lb. boxes containing two 5-lb. vacuum-packed packages containing frozen GEO BROWN ALL BEEF HOTDOGS and PACKED ON with various dates since approximately May 30, 2024, represented on the label.

    The products subject to recall bear establishment number EST. 47635 inside the USDA mark of inspection. These items were shipped to restaurant and hotel locations in Ohio and West Virginia.

    The problem was discovered when FSIS was notified by a state public health partner about these products. FSIS investigated and determined that the hot dog products were produced and distributed without the benefit of federal inspection.

    What to do

    There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

    FSIS is concerned that some product may be in restaurants or hotels refrigerators or freezers. Restaurants and hotels are urged not to serve these products. These products should be thrown away or returned to the place of purchase.

    Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov.

    For consumers whoneed to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

  14. Both products fail to meet federal flammability standards

    By Mark Huffman of ConsumerAffairs
    July 16, 2024

    PhotoTwo different manufacturers are recalling childrens sleepwear because they dont meet federal flammability standards.

    JUVENNO KIDS is recalling 16,820 units of childrens button-up short-sleeve.shorts two-piece pajama sets because they violate the flammability standards for childrens sleepwear, posing a risk of burn injuries to children.

    This recall involves childrens two-piece pajama sets sold in champagne, light purple, and peach colors. The pajama set consists of a short-sleeve, button-up top and matching shorts. All colors have white trim on the sleeves, collar, shirt pocket, placket with buttons down the center seam of the shirt, shirt hem, and shorts hem.

    On the front permanent label attached to the pajamas is the size and 100% Polyester, and on the back are washing instructions and MADE IN CHINA.

    What to do

    Consumers should immediately take the recalled pajamas away from children, stop using them, and contact JUVENNO KIDS to receive a full refund.

    Consumers should destroy the garments by cutting the top and bottom in half and dispose of them in accordance with local and state recycling laws.

    Consumers should send the recalling firm a photo of the destroyed garments by email at 603262718@qq.com or via message to JUVENNO KIDS on Temu.com to receive a refund. JUVENNO KIDS is contacting all known purchasers directly.

    Lovely Angel nightgowns

    Lovely Angel is recalling more than 4,300 units of childrens lace nightgowns because they fail to meet federal flammability standards and can pose a burn hazard to children.

    This recall involves Lovely Angel childrens lace nightgowns sold in six colors, including black, lavender, watermelon, beige, green and red. The short-sleeved nightgowns have white lace trim on the chest area and on the bottom hem, and a white ribbon bow at the collar.

    They were sold in childrens sizes ranging from 3Y to 12Y. A side seam label states the following: 100% Rayon, washing instructions, manufacturer name Tong Tai clothing co., Ltd, Made in china, Huang mei, HuBei, lot number 021123, and manufacture date 11/2023.

    What to do

    Consumers should immediately take the recalled nightgowns away from children, stop using them, and contact Lovely Angel to receive a full refund. Consumers should destroy the garments by cutting them in half and disposing of them in accordance with local and state recycling laws. Consumers should send the recalling firm a photo of the destroyed garment at wangmaxime@163.com or via Lovely Angels online store to receive a refund. Lovely Angel is contacting all known purchasers directly.

  15. The company says they may not charge properly

    By Mark Huffman of ConsumerAffairs
    July 15, 2024

    PhotoBaxter International has issued an urgent medical device recall for Life2000 ventilators because of potential battery charger damage that can prevent the device from charging.

    Baxter has received one serious injury complaint potentially related to this issue and is working with customers to replace affected Life2000 ventilator devices.

    Damage to the battery charger dongle prevents the ventilators internal battery from charging. If the Life2000 ventilator fails to charge or has intermittent charging behavior, this may leave the patient unable to use the device.

    For patients requiring ventilator support, the inability to use the device may result in oxygen desaturation episodes that range from mild to potentially life-threatening. Patients should always have an alternate means of ventilation or oxygen therapy available.

    What to do

    Baxter has contacted affected customers, instructing them to inspect the condition of the battery charger dongle and confirm the device is charging properly. If damage is observed or the battery is not charging properly, patients should contact Baxter Home Care Customer Service to have the device replaced immediately.

    If no damage is observed and the battery is charging properly, patients may continue to use the ventilator and Baxter will replace the device at the patients next scheduled in-home visit with a clinical trainer.

    The Urgent Medical Device Recall applies to the Life2000 ventilator with product code MS01-0118 with an attached battery charger dongle. The impacted ventilators were distributed in the United States between Aug. 21, 2023 and April 2, 2024.

    Baxter has notified the U.S. Food and Drug Administration (FDA) of this action. Any product quality complaints or adverse events experienced with the use of these products may be reported using one of the following options:

    Calling Baxter Home Care Customer Service at 800-426-4224, option 3 between the hours of 7:30 a.m. and 6 p.m. central time, or Baxter Clinical Support at 800-397-9071, which is available 24 hours a day.

    Reporting to the FDA MedWatch Serious Injury Reporting Program:

    Online: By completing and submitting the report online at: https://www.accessdata.fda.gov/scripts/medwatch/ o Regular mail or fax: Download the form from www.fda.gov/MedWatch/getforms.htm or call 800-332-1088 to request a reporting form, then complete and mail it to the address on the pre-addressed form or submit by fax to 800-332-0178.

  16. The heaters can turn on by themselves

    By Mark Huffman of ConsumerAffairs
    July 12, 2024

    PhotoAtomi is recalling nearly 100,000 smart heaters because they can turn on without user input, posing fire and burn hazards. Atomi has received one report of the heater turning on without user input but no injuries have been reported.

    The recall involves Atomi Smart Heaters, tower models AT1323, AT1481, AT1520 and AT1632; tabletop models AT1482 and AT1521; and wall heater model AT1635.

    These portable electric heaters were sold in black, silver or white color, depending on the model. The tower heater models measure about 26-28 inches tall and 8-11 inches wide. The tabletop heater models measure about 18 inches tall and eight inches wide.

    The wall heater models measure about 17 inches tall and 23 inches wide. The model number can be found on a product identification sticker on the bottom of the unit.

    The heaters were sold at Amazon, Ace Hardware, Atomiusa.com, Best Buy, BJs Wholesale Club, Costco, Hammacher Schlemmer, Home Depot, Lowes.com, Menards, Sam's Club and Walmart stores nationwide from October 2019 through April 2024 for between $80 and $150, depending on the model.

    What to do

    Consumers should immediately stop using the recalled heaters, unplug the units, and follow the instructions online at www.atomiheaterrecall.com to receive a full refund.

    Consumers will be asked to cut the unplugged units power cord and upload a photograph of the cut cord, as well as a photograph of the manufacturers label on the underside of their units during the registration process.

    Consumers may also call Atomi toll-free at 888-770-7140 from 7:30 a.m. to 5 p.m. CT Monday through Friday, or online at www.atomiheaterrecall.com or www.atomismart.com and click on Recalls at the bottom of the page for more information.

  17. There have been three reports of fires caused by the lights

    By Mark Huffman of ConsumerAffairs
    July 11, 2024

    PhotoBest Lights has issued a recall for 760,000 High Bay LED light fixtures because of a potential fire hazard. Plastic pins securing the LED board can degrade, allowing the energized LED board to come loose and contact the lens or combustible materials, posing a fire hazard.

    The recall involves Best Lighting Products LEDFHB line of high bay light fixtures in 90, 105, 135, 178, 180, 215, 265, 320 and 425 watts. These lights were sold in white, and are typically used in commercial settings, such as warehouses and facilities with high ceilings.

    The following model numbers are included in this recall: LEDFHB90, LEDFHB105, LEDFHB135, LEDFHB178, LEDFHB180, LEDFHB215, LEDFHB265, LEDFHB320 and LEDFHB425. The model name and number can be found on a label on the back of the recalled fixtures.

    The company has received three reports of fires involving the recalled fixtures. No injuries have been reported.

    What to do

    Consumers should immediately inspect the fixture for any sign of pin degradation, a loose LED board, or discoloration of the lens. Consumers should immediately stop using light fixtures that show any sign of a loose LED board or discoloration of the lens, and turn the circuit off.

    Customers can contact BLP for more information, and register online at www.highbayrecall.net to schedule a free inspection and on-site repair to replace the plastic pins with metal pins.

    Consumers may also contact Best Lighting Products toll-free at 888-204-9905 anytime, or online at www.highbayrecall.net or www.bestlighting.net and click on Recall at the bottom of the page for more information.

  18. 2006 through 2009 models are included

    By Mark Huffman of ConsumerAffairs
    July 11, 2024

    PhotoBMW of North America is recalling 394,029 2006-2011 3 Series Sedan 324i, 325i, 325xi, 328i, 328xi, 330i, 330xi, 335i, 335xi, 2006-2012 3 Series Sportswagon 325xi, 328i, 328xi, and 2009-2011 3 Series Sedan 335d vehicles.

    The original steering wheel may have been replaced with a sport or M-sport steering wheel equipped with an inflator that can explode during deployment. An inflator explosion may result in sharp metal fragments striking the driver or other occupants, resulting in serious injury or death.

    What to do

    Dealers will inspect and replace the driver's airbag module as necessary, free of charge. Owner notification letters are expected to be mailed by August 23, 2024. Owners may contact BMW customer service at 1-800-525-7417.

    Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.nhtsa.gov.

  19. The company said a front seat airbag does not deploy

    By Mark Huffman of ConsumerAffairs
    July 10, 2024

    PhotoChrysler has issued a recall for 332,000 vehicles because a front seat airbag does not deploy as intended and can increase the risk of injury in a crash.

    Included in the recall are certain 2017-2024 Alfa Romeo Giulia, 2018-2025 Alfa Romeo Stelvio, 2019-2023 Fiat 500X, Jeep Renegade, and 2024 Fiat 500E vehicles. A seat belt buckle switch sensor may be improperly connected, preventing the front seat airbag from deploying as intended.

    What to do

    Dealers will repair the connection, free of charge. Owner notification letters are expected to be mailed by August 22, 2024. Owners may contact FCA US, LLC customer service at 1-800-853-1403. FCA US, LLC's number for this recall is 82B.

    Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 1-888-327-4236 (TTY 1-800-424-9153), or go to www.nhtsa.gov.

  20. Consumers are urged to stop using the hair dryers and get a free replacement

    By Mark Huffman of ConsumerAffairs
    July 9, 2024

    PhotoFocusee is recalling nearly 40,000 Tideway High-Speed Hair Dryers. According to the Consumer Product Safety Commission (CPSC), the handheld hair dryers lack an immersion protection device, posing an electrocution or shock hazard to consumers if they fall into water when plugged in.

    The CPSC has determined that hair dryers not equipped with the integral immersion protection present a substantial product hazard. To date, no incidents have been reported.

    The hair dryers come with a nozzle, and were sold in white with gold on the bottom of the handle. Tideway is printed on the front of the handle. The hair dryers have an LED ring on them that corresponds to the different temperature settings of the hair dryer. Red represents hot air, orange represents warm air, blue represents cold air, and green represents hot and cold cycles.

    The hair dryers were sold online at TikTokShop.com, Shopify.com and other websites from November 2023 through March 2024 for about $170.

    What to do

    Consumers should immediately unplug and stop using the recalled hair dryers, and

    contact Tideway Shop to receive a free replacement. Consumers should destroy the recalled hair dryers by unplugging the hair dryer, cutting the cord and disposing of them in accordance with local and state recycling laws, and send an image of the destroyed hair dryer to info@tideway.shop or tidewayshopify@gmail.com. Upon receipt of the photo, Focusee will send the customer a replacement hair dryer with an immersion protection device.

    Consumers may contact Tideway Shop at collect 209-267-4999 from 8 a.m. to 7 p.m. CT Monday through Friday or 8 a.m. to 6 p.m. CT Saturday and Sunday, email at info@tideway.shop or tidewayshopify@gmail.com, or online at https://tideway.shop/ and click on Recall for more information, or click on https://tideway.shop/recall.