Browse through 2,317 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Stryker recalled 289 Arise 1000EX mattresses on October 31, 2025. The recall affects products sold nationwide due to potential incompatibility with MV3 beds. Users should stop using these mattresses immediately.
Philips North America recalled over 1.9 million IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to sound alarms, posing a serious risk to patients. Healthcare providers must stop using these devices immediately and follow recall instructions.
Trifecta Pharmaceuticals recalled 33,000 containers of Globe Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. Consumers should stop using the product immediately to avoid potential risks. Healthcare providers are advised to contact the company for further guidance.
Dynarex Corporation recalled 8,184 bottles of Dynagel Moisturizing Wound Hydrogel on October 31, 2025. The recall follows deviations from current Good Manufacturing Practices (cGMP). Consumers should stop using the product immediately and consult healthcare providers for guidance.
Philips North America recalled 1,913,441 IntelliVue MP50 monitors on October 31, 2025. The monitors may fail to alarm, posing a high risk to patient safety. Healthcare providers must stop using the devices immediately and follow recall instructions.
First & Last Tavern recalled 30 cases of Puttanesca Sauce on October 31, 2025. The product may be contaminated with Clostridium botulinum, a toxin that can cause severe illness. Consumers should stop using the sauce immediately and contact the company for a refund.
First & Last Tavern recalled 30 cases of marinara sauce on October 31, 2025. The sauce may be contaminated with Clostridium botulinum, posing a high health risk. Consumers should not consume the product and seek refunds or replacements.
Blossom Pharmaceuticals recalled 9,600 containers of Lanashield Skin Barrier on October 31, 2025 due to cGMP deviations. Consumers and healthcare providers should stop using the product immediately. The recall affects products distributed nationwide in the USA.
Trifecta Pharmaceuticals USA recalled 12,150 bottles of Globe Clotrimazole Cream on October 31, 2025. The recall stems from deviations in current Good Manufacturing Practices (cGMP). Consumers should stop using the cream immediately and contact their healthcare providers.
Nivagen Pharmaceuticals recalled 7,920 bottles of Zinc Oxide Ointment on October 31, 2025. The recall follows cGMP deviations that could impact product safety. Consumers should cease use immediately and consult healthcare providers for advice.
Stryker Corporation recalled 39,148 BrainPath devices on October 31, 2025, due to a latex allergy risk. The tape used to secure components contains latex, despite being labeled latex-free. This recall affects devices distributed worldwide, including the U.S. and multiple countries.
Dynarex Corporation recalled 2,592 bottles of WeCare Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers and healthcare providers must stop using the ointment immediately and seek guidance.
Stryker Medical recalled 286 MV3 bariatric beds on October 31, 2025. The beds may not be compatible with Arise 1000EX mattresses, posing risks to patients. Healthcare providers and patients must stop using the beds immediately.
Philips North America recalled 1,913,441 IntelliVue MP80 monitors on October 31, 2025. The devices may fail to alarm, presenting a high risk to patient safety. Healthcare providers and patients should stop using the monitors immediately.
Cipla USA recalled 4,438 cartons of Phytonadione Injectable Emulsion on October 31, 2025. The product failed stability specifications, raising concerns about its safety. Consumers and healthcare providers must stop using the product immediately and seek guidance.
Werner Paddles recalled Stealth and Covert kayak paddles on October 30, 2025. The paddles can break during use, creating a drowning hazard. Consumers should stop using the paddles and seek a refund immediately.
Modera recalled Pack N Play mattresses on October 30, 2025, due to serious entrapment hazards. These mattresses may not fit securely in play yards, risking suffocation. Consumers must stop using the mattresses and contact Modera for refunds.
Harppa recalled 50,000 5-in-1 convertible high chairs on October 30, 2025. The chairs lack required restraints, posing fall and entrapment risks to children. The recall affects models with BHC001 and production batch 202408 labels.
Avenco and Novilla recalled mattresses on October 30, 2025, due to a fire hazard. The mattresses violate mandatory flammability standards, posing a risk of serious injury or death. Consumers should stop using the products immediately and contact the manufacturer for a remedy.
WLIVE expanded its recall of 16-drawer dressers on October 30, 2025. Consumers reported serious injury risks due to instability if not anchored. The dressers violate safety standards and pose hazards to children.