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Consumer Daily Reports

The second-row side door lock may malfunction

By Mark Huffman Consumer News: BMW recalls nearly 41,000 X3 sDrive30i and X3 xDrive30i vehicles of ConsumerAffairs
February 25, 2025

BMW of North America is recalling 40,736 2022-2024 X3 sDrive30i and X3 xDrive30i vehicles. The second-row seat side door locking modules may not function properly and allow the doors to be unlocked with a single motion. Doors that can be inadvertently unlocked and unlatched may open unexpectedly, increasing the risk of injury to rear seat occupants.

As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 206, "Door Locks and Door Retention Components."

What to do

Dealers will replace the second-row seat side door locking modules, free of charge. Owner notification letters are expected to be mailed April 14, 2025. Owners may contact BMW customer service at 800-525-7417.

Owners may also contact the National Highway Traffic Safety Administration Vehicle Safety Hotline at 888-327-4236 (TTY 888-275-9171) or go to nhtsa.gov.

To determine if your vehicle is included in this recall, check the NHTSA recall page.

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Posted: 2025-02-25 15:35:37

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Consumer News: Merck’s new cancer drug option, Keytruda Qlex, wins FDA approval

Mon, 22 Sep 2025 16:07:07 +0000

The new option offers convenience and flexibility in treatment settings

By Mark Huffman of ConsumerAffairs
September 22, 2025
  • FDA approves Keytruda Qlex, a subcutaneous injection version of the widely used cancer therapy Keytruda

  • Patients can now receive treatment in as little as one to two minutes, compared to a 30-minute IV infusion

  • New option offers greater convenience and flexibility in treatment settings, from hospitals to local clinics


The U.S. Food and Drug Administration (FDA) has approved Keytruda Qlex (pembrolizumab and berahyaluronidase alfa-pmph), a new subcutaneous form of Mercks flagship cancer immunotherapy Keytruda. This marks the first time patients across most of Keytrudas 38 cancer indications will have access to the drug in an injection form rather than an intravenous (IV) infusion.

Keytruda Qlex can be administered by a healthcare provider in just one minute every three weeks or two minutes every six weeks. Thats a major time savings compared to the 30-minute IV infusion required for traditional Keytruda.

This approval is significant for patients and health care providers like me who have been using immunotherapies for years to treat certain cancers, said Dr. J. Thaddeus Beck, oncologist and medical director of the Highlands Clinical Trials Office. Subcutaneous pembrolizumab provides faster administration, two dosing options, and more choices for where patients can receive care.

Comparable effectiveness and safety

In pivotal clinical trials, Keytruda Qlex showed similar effectiveness and safety compared to IV Keytruda. Patients with advanced lung cancer who received the injection saw response rates and survival outcomes nearly identical to those receiving the infusion.

The new formulation was developed with the help of biotechnology company Alteogen Inc., whose enzyme allows pembrolizumab to be delivered under the skin instead of through a vein.

For patients who struggle with vein access or who dont have a port in place, the subcutaneous injection may simplify treatment. It also gives patients and providers more flexibility in choosing where treatment takes place, whether in a hospital infusion center, a doctors office, or a community clinic.

This is about giving patients options and helping them manage treatment in a way that best fits their needs, said Dr. Marjorie Green, senior vice president and head of oncology at Merck Research Laboratories.

Safety considerations

As with IV Keytruda, Keytruda Qlex carries risks of serious immune-related side effects, which may affect organs such as the lungs, liver, or kidneys, and in rare cases can be life-threatening.

It is not recommended for certain patients, including those with hypersensitivity to its components or pregnant women due to potential risks to the fetus. Patients are encouraged to discuss the benefits and risks with their healthcare team.

Merck expects Keytruda Qlex to be available in the United States in late September. Patients and caregivers can ask their oncologists if the new injection option is right for them.


Read More ...


Consumer News: Urgent recall issued for fish product sold at Costco in 34 states

Mon, 22 Sep 2025 13:07:16 +0000

Kirkland Signature brand Ahi Tuna Wasabi Poke may be contaminated with listeria

By Mark Huffman of ConsumerAffairs
September 22, 2025

  • Western United Fish Company is recalling 3,314 pounds of Kirkland Signature Ahi Tuna Wasabi Poke due to possible Listeria monocytogenes contamination.

  • The recalled product was sold on Sept. 18 in the deli section at Costco warehouses across 34 states.

  • No illnesses have been reported yet. Customers should not eat the product, dispose of it immediately, and request a full refund at Costco. For questions, contact Annasea Foods at (425) 558-7809 or info@annasea.com

Western United Fish Company, dba Annasea Foods Group, has issued an urgent recall of 3,314 pounds of Kirkland Signature brand Ahi Tuna Wasabi Poke, Costco Item Number of 17193, with the Sell By Date of 9/22/2025.

The recall was issued because the green onions used in the product have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

The affected Ahi Tuna Wasabi Poke product is packaged in clear plastic clamshell containers and has the Kirkland Signature brand label with the Pack Date of 9/18/2025 and Sell By Date of 9/22/2025.

The product was sold at the deli section from Costco Warehouse stores in the following states on Sept. 18, 2025: Alabama, Alaska, Colorado, Connecticut, Delaware, Florida, Georgia, Idaho, Indiana, Louisiana, Maine, Maryland, Massachusetts, Minnesota, Mississippi, Missouri, Montana, Nebraska, New Hampshire, New Jersey, New Mexico, New York, North Carolina, Ohio, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, and Wisconsin.

No illnesses have been reported to date.

What to do

This recall was initiated after the company was notified by its green onion supplier of a Listeria monocytogenes positive test result in the green onions, which were used only in Ahi Tuna Wasabi Poke on Sept. 17. The company said it is continuing to work with its green onion supplier to determine the root cause.

Consumers should not consume this affected product and dispose of it immediately and visit your local Costco for a full refund.

Please call Annasea Foods Group at (425) 558-7809, 7:00am - 3:30pm Pacific Time, Monday Friday, or email info@annasea.com if you have any issues or concerns.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.


Read More ...


Consumer News: Amazon’s Prime marketing campaign goes on trial in Seattle

Mon, 22 Sep 2025 13:07:16 +0000

The Federal Trade Commission is suing the retailer for alleged deceptive practices

By Mark Huffman of ConsumerAffairs
September 22, 2025
  • A landmark trial begins, as the U.S. Federal Trade Commission moves forward with allegations that Amazon systematically misled consumers into signing up for its Prime membership.

  • The FTC claims Amazon used deceptive interface designs so-called dark patterns to enroll users in automatically-renewing Prime subscriptions without meaningful consent, and made cancellation needlessly difficult.

  • In recent pretrial rulings, a judge found Amazon violated the Restore Online Shoppers Confidence Act (ROSCA) by collecting billing information before disclosing key membership terms, and also held that Amazon executives could be held personally liable if the FTCs allegations are proven.


Millions of people are members of Amazons Prime but the Federal Trade Commission claims some are members against their will and find it hard to cancel.

After years of investigation, legal wrangling, and preliminary rulings, the trial in FTC v. Amazon.com Inc. begins this week in U.S. District Court in Seattle. The FTC is seeking remedies for what it describes as years-long deceptive practices tied to Amazons Prime program.

The allegations include:

  • Deceptive signup flows: The complaint says that Amazon routinely presents consumers with options that make Prime subscription a default or overwhelming choice. Buttons enrolling customers tend to be large, prominently displayed, and worded to emphasize benefits (free shipping, trial, etc.), while the option to decline is obscured by size, position, or weaker language.

  • Billing before full disclosure: According to the FTC, in many cases, Amazon collected payment information from prospective Prime members before clearly disclosing all the terms of the subscription including its automatic renewal, cancellation requirements, or full cost.

  • Iliad cancellation scheme: The FTC alleges Amazon made the cancellation process overly long, labyrinthine, and discouraging. Internally, this complex cancellation path has been referred to as Iliad involving multiple pages, numerous clicks, and many choices or offers intended to persuade customers to stay.

Whats at stake

  • The FTC is seeking civil penalties, injunctive relief (changes to how the Prime subscription and cancellation flows are structured), and possibly consumer refunds for people harmed by these alleged practices.

  • Amazon strongly denies the claims, arguing that its disclosures are clear, that customers have the requisite information to make informed decisions, and that it has taken steps to simplify cancellation flows in response to feedback and regulatory pressure.

U.S. District Court Judge John Chun has already granted the FTC significant pretrial victories, ruling that Amazon violated ROSCA (Restore Online Shoppers Confidence Act, a U.S. federal law passed in 2010), rejecting motions to dismiss major parts of the FTCs case, and allowing claims of executive liability to move forward.

The case builds on evolving legal scrutiny over dark patterns and subscription models with auto-renewal features. Regulators in the U.S. and abroad have increasingly focused on such practices as potentially deceptive under consumer protection laws.

The outcome of the jury trial may hinge on whether the FTC can prove that users were tricked in a legally meaningful way showing that Amazons interfaces and disclosures failed to give consumers a clear, informed choice.


Read More ...


Consumer News: Federal flood insurance program faces Sept. 30 deadline

Mon, 22 Sep 2025 04:07:16 +0000

If the program isn't reauthorized by Congress, major elements could disappear

By James R. Hood of ConsumerAffairs
September 22, 2025
  • The flood insurance program faces a Sept. 30 deadline. Major elements can disappear without Congressional action.
  • Participation in the program is already extremely low and sinking fast because of rising premiums.
  • Many homes that flood repeatedly drive up a big share of the program's costs.

If Congress does not reauthorize the National Flood Insurance Program (NFIP) by September 30, major parts of the program will expirea lapse that could cause major problems in the mortgage industry.

In past NFIP lapses, borrowers were not able to purchase flood insurance to close, renew or increase loans secured by property that required flood insurance. The Congressional Research Service (CRS) estimated that during a lapse in June 2010, each day more than 1,400 home sale closings were canceled or delayed. That represents more than 40,000 sales each month.

This is an urgent pocketbook issue for many in our state," said Sen. Cory Booker (D-NJ). He and other lawmakers have been looking for a long-term solution to funding the program but their efforts have failed so far.The House has passed. H.R. 5371, legislation that would fund much of the governmentand reauthorize the NFIP until Nov. 21. However, the Senate has rejected that legislation.

Lawmakers are considering lowering caps to annual premium increases, allowing policyholders to pay monthly premiums rather than annual ones, and higher coverage limits for flood damage, among other changes.

Participation low and declining fast

Just 3.3% of U.S. homes had active National Flood Insurance Program (NFIP) policies as of Nov. 2024, marking a second-year of declines and a 0.2% drop from the prior year, according to a report frominsurance website ValuePenguin.

NFIP policies account for the vast majority of flood insurance and provides thebasics, but a smaller share of homeshave private flood insurance that can offerbroader coverage.

"Two years of back-to-back decreases in active flood insurance policies indicates that many homeowners arent fully aware of the growing risks of flooding," said Divya Sangameshwar, ValuePenguin's insurance expert, in the report.

The situation is even worse in 26 states where fewerthan 1% of homes have flood insurance, including Pennsylvania, Colorado and Michigan.

Efforts to find long-term financing fail

If the NFIP is allowed to lapse, the CRS has said that flood insurance contracts entered into before the expiration would continue until the end of their policy term of one year. The authority for the NFIP to borrow funds from the U.S. Treasury would be reduced from $30.425 billion to $1 billion.

Despite repeated efforts, Congress has been unable to enact a long-term NFIP reauthorization. Traditionally, the NFIP has been reauthorized in must-pass short-term and long-term spending measures. The CRS said that the NFIP has been reauthorized in such legislation 33 times since 2017. The last long-term reauthorization was the Biggert-Waters Flood Insurance Reform Act of 2012.

Fast-rising premiums

Under current law, National Flood Insurance premiums can increase by no more than 18% a year. Some lawmakers have suggestedreducing that capto 9%.

The National Flood Insurance Program is distressed by premiums driven by a small share of extremely high-risk properties that repeatedly flood.

As premiums rise, more policyholders move to private plans or forgo flood insurance because they can no longer afford it. Smaller subscriber pools inflate risk and drive up premiums, pushing more policyholders away in a vicious cycle not unlike the one faced byNew Jerseys State Health Benefits Programfor local government workers.


Read More ...


Consumer News: TikTok soon to be 'under American control,' White House says

Mon, 22 Sep 2025 04:07:15 +0000

U.S. will take six of seven board seats and Oracle will take control of the site's algorithm

By James R. Hood of ConsumerAffairs
September 22, 2025
  • White House says US companies will oversee TikToks algorithm and Americans will hold six of seven board seats for US operations.
  • Oracle, chaired by Trump ally Larry Ellison, will lead data and privacy protections.

  • Trump and Xi discussed TikToks future, but Beijing has not confirmed approval of the deal.


White House signals breakthrough in talks

The White House announced over the weekend that US companies will take control of TikToks algorithm and that six of seven board seats in the apps US operations will be held by Americans. Press secretary Karoline Leavitt said a deal could be signed in the coming days, though Chinese officials have yet to comment publicly.

Speaking on the Fox News program Saturday in America, Ms. Leavitt said that we are 100 percent confident that a deal is done, but added in the same breath that the deal had not yet been signed, the New York Times reported.She said that could happen in the coming days.

The move follows years of negotiations over whether TikTok could continue to operate in the United States amid concerns over its Chinese parent company, ByteDance. The app had previously faced the threat of a ban unless its US business was sold.

Oracle to oversee data and privacy

Leavitt saidthat US tech giant Oracle will lead TikToks US data and privacy safeguards. Oracles founder and chair, Larry Ellisonlong a political ally of President Trumpwill play a central role.

The data and privacy will be led by one of Americas greatest tech companies, Oracle, and the algorithm will also be controlled by America as well, Leavitt told Fox News. She added that all of those details have already been agreed upon, with only a final signature needed to seal the deal.

The Ellison family has gained growing influence in US media, with Larry Ellisons son, David, recently acquiring Paramount, owner of CBS News.

Mixed signals from China

President Trump said he and Chinese President Xi Jinping discussed TikTok in a phone call and both approved the deal. He described the exchange as productive in a Truth Social post.

But Beijings response has been less clear. Chinas Commerce Ministry said it welcomed negotiations in accordance with market rules and emphasized that any solution must comply with Chinese law. State news agency Xinhua quoted Xi as welcoming talks, without confirming a final agreement, according to aBBC report.

Dispute over the algorithm

A major sticking point in negotiations has been who controls TikToks powerful recommendation algorithm, which shapes content for its 170 million American users. While Trump sidestepped questions about whether a new algorithm would be needed, the White House has now insisted that control will rest firmly in US hands.

Legal and political backdrop

In January, the US Supreme Court upheld a 2024 law banning TikTok unless ByteDance divested from its US operations. The app briefly went offline before the deadline was pushed back. Trump, who initially called for TikTok to be banned during his first term, shifted course in 2024 and embraced the platform to reach younger voters in his presidential campaign.

The Justice Department has previously warned that TikTok posed a national security threat of immense depth and scale, citing concerns about user data access.


Read More ...


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