These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
2,775 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
Mercedes-Benz USA recalled the 2025 EQS SUV 580 4MATIC on April 5, 2026. The recall affects vehicles due to battery management software issues that can cause a sudden loss of drive power. This malfunction increases the risk of a crash, prompting immediate action by the company.
BMW recalled certain 2025 X3 30 xDrive vehicles due to potentially damaged front brake discs. This defect may impair braking, increasing the risk of a crash. Owners should expect notification letters by June 6, 2025.
Sangohe expands its 2026 recall of adult portable bed rails 504E and 504Q due to entrapment and asphyxiation risk. The recall cites noncompliance with the mandatory standard and missing warning labels. Stop using the recalled rails and pursue a full refund by contacting Sangohe.
Beestech's Bee-210316-01 spiral tower toy sold on Amazon is recalled after the CPSC found it poses a choking hazard for children under three. The recall notes the toy contains small balls and violates the Small Ball Ban. Stop using the toy immediately and contact Beestech for a full refund.
Gavoyeat recalled 50-ring Halloween Light-Up Rings sold on Amazon by CSZWEICD on April 2, 2026. The recall cites a battery ingestion hazard from an accessible button cell battery in the ring’s housing. Stop using the recalled rings and return them for a full refund by emailing recalledgavoyeat@yeah.net.
Sam's Club recalls Member's Mark Valentine pajama sets due to burn risk and a violation of mandatory flammability standards for children's sleepwear. The recall covers sizes XS through XL sold online between December 2025 and January 2026 for about $14. Consumers should stop using the pajamas immediately and contact Sam's Club for a full refund.
E Mishan recalls Granitestone Diamond Pro Blue stainless sauté pans sold online at Granitestone's official site in a 2-piece set. The metal cap on the screw that connects the pan to the handle can detach and eject when heated, creating burn and impact hazards. Consumers should stop using the recalled pans immediately and contact E Mishan for a full refund.
Tuymec Minoxidil Hair Growth Kit sold on Amazon by DrHealBeauty is recalled for non-child-resistant packaging. The kit contains two black spray bottles with 5% minoxidil and BIOTIN labels. Consumers should stop using the product immediately and contact DrHealBeauty for a free empty replacement bottle with a child-resistant closure.
Coluans recalled Christmas Light-Up Rings sold on Amazon by BUDI Official. The recall centers on a battery ingestion hazard from three preinstalled button cell batteries visible through the ring’s clear casing. Stop using the rings immediately and return them for a full refund by emailing BUDIrecall@outlook.com with a photo of the disposed product.
ELENKER recalled three models of portable bed rails sold on Amazon by Fuzhou Shiahaha Cultural Industry Development. The rails can entrap users or create a gap with the mattress, posing a risk of suffocation and death, and they lack required hazard warnings. Consumers should stop using the rails immediately and contact the company for a full refund.
HTRC and Haisito T400 battery chargers sold by Huizhou Haitan Technology are recalled. The recall warns that the chargers can ignite or cause a connected battery to ignite, posing a fire risk and a danger of serious injury or death. Stop using the chargers now and contact the manufacturer for a full refund and return instructions.
OCUN NA recalled Condor HMS Triple Carabiners sold online and through climbing retailers after the gate may fail to close automatically. The carabiner features an independent internal wire gate and a triple locking action. Stop using the recalled carabiner immediately and contact OCUN NA for a free replacement.
TecFlox recalled its Minoxidil Topical Solution hair growth serum bottles on April 2, 2026. The packaging is not child-resistant, violating the Poison Prevention Packaging Act. Consumers should stop using the product immediately, store it out of reach of children, and email TecFloxrecall@outlook.com to receive free replacement bottles. Only bottles with serum remaining will be replaced; dispose of
General Motors recalled certain 2024 Chevrolet Silverado EV and 2024-2025 GMC Sierra EV pickup trucks due to a seat belt safety issue. The recall affects vehicles still in dealer inventory, with no owner letters mailed. Owners can contact GM customer service for further assistance.
General Motors recalled certain 2025 Chevrolet Equinox EVs on April 1, 2026. The adaptive cruise control may fail to engage the brakes due to incorrect software. This defect increases the risk of a crash, impacting all-wheel drive electric vehicles.
Millions of eye drop bottles sold at CVS, Walgreens, Kroger, and other major pharmacies may not be sterile. K.C. Pharmaceuticals of Pomona, California never verified that eight of its over-the-counter eye drop products met sterility standards, the FDA warned. A nearly identical manufacturing failure in 2023 left patients blind, cost others their eyes, and killed at least three people. Consumers should stop using the products and return them for a full refund.
HEYTEA USA INC recalls 12,677 cartons of Coconut Drink 1 sold for catering establishments in multiple states after undeclared milk was found. The product contains milk not listed on the label. Consumers should not consume the product and contact HEYTEA USA INC for refund or replacement by email.
Biocon Pharma Inc. recalled 88,008 bottles of Prazosin Hydrochloride capsules, 1 mg, 100-count bottles, nationwide in the United States. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or a healthcare provider for guidance.
Biocon Pharma Inc. recalled 28,157 bottles of PRAZOSIN HYDROCHLORIDE capsules, distributed nationwide in the USA. The recall cites cGMP deviation due to detection of N-nitroso-prazosin impurity C above acceptable limits. Stop using the product immediately and contact Appco Pharma LLC or your healthcare provider for guidance.
Biocon Pharma Inc. recalled 58,896 bottles of Prazosin Hydrochloride Capsules, USP, 2 mg, 100-count bottle. The product was distributed nationwide in the USA and manufactured by Appco Pharma LLC. A cGMP deviation detected N-nitroso-prazosin impurity C above acceptable limits. Consumers and healthcare providers should stop using this product immediately and contact Appco Pharma LLC or their health‑