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.
Stryker Communications recalled 40 surgical light systems on July 15, 2025, due to potential powder coating chipping. This defect increases risks for healthcare providers and patients. Affected products were distributed nationwide, including Texas, Illinois, and New York.
WLIVE recalled its 15-drawer fabric dressers on July 10, 2025. The recall affects models that pose tip-over and entrapment hazards. Consumers should stop using these dressers immediately if not anchored to a wall.
Haoyunm recalled braided crib bumpers on July 10, 2025, due to suffocation hazards. The crib bumpers violate federal safety regulations. Consumers should stop using them immediately and seek a refund.
Dearlomum recalled retractable safety gates on July 10, 2025. The gates pose a serious entrapment hazard to children, potentially leading to injury or death. About 10,000 units were sold on Amazon and other retailers.
SPPTTY recalled kids bicycles on July 10, 2025, due to lead poisoning risks. The bicycles exceed federal lead content limits, posing serious health hazards to children. Consumers should stop using the bicycles and seek refunds immediately.
AUGNORYE recalled padded crib bumpers on July 10, 2025, after reports of suffocation hazards. The bumpers violate federal safety regulations. Consumers should stop using them immediately and request a refund.
Biofire Defense recalled 130 kits of the FilmArray NGDS Warrior Panel on July 10, 2025. The recall is due to an increased risk of internal control failures when testing positive blood cultures. These failures could delay results and require additional diagnostic workups.
Boothwyn Pharmacy recalled 8 vials of Fluorescein 2% Ophthalmic Solution on July 9, 2025. The recall occurred due to the drug being subpotent, posing potential health risks. Consumers should stop using the product immediately and seek guidance from their healthcare provider.
Boothwyn Pharmacy recalled 642 vials of Semaglutide injection on July 9, 2025. The recall follows the discovery that the drug is subpotent. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Boothwyn Pharmacy recalled 186 vials of Semaglutide, 2.5 mg/mL injection on July 9, 2025. The product is subpotent and poses a risk to consumers. Healthcare providers and consumers should stop using this product immediately.
Boothwyn Pharmacy recalled 648 vials of Semaglutide injection on July 9, 2025. The product is subpotent and poses a high hazard risk. Consumers should stop using the product immediately and contact their healthcare provider.
Boston Scientific Neuromodulation recalled 25,260 deep brain stimulation systems on July 8, 2025, due to wire break issues. Users may experience loss of therapy and other serious complications. Patients should stop using the devices immediately and seek further instructions.
Medline Industries recalled approximately 6.67 million alcohol prep pads on July 7, 2025. The recall stems from isopropyl alcohol levels falling below the labeled concentration. Consumers should stop using the product immediately and seek guidance from healthcare providers.
Rite Aid recalled 984,000 first aid alcohol prep pads on July 7, 2025, due to subpotent isopropyl alcohol levels. The affected product may not effectively disinfect, posing health risks to users.
Walmart recalled 3.46 million ReliOn Sterile Alcohol Swabs on July 7, 2025. The swabs contain isopropyl alcohol levels below the labeled concentration. Consumers should stop using the product immediately.
CURAD recalled 1,639,996 alcohol prep pads on July 7, 2025. The recall addresses subpotent isopropyl alcohol levels that fall below labeled concentration. Consumers should stop using these products immediately.
Good Neighbor Pharmacy recalled 66,000 alcohol prep pads on July 7, 2025. The product failed to meet isopropyl alcohol concentration standards. Consumers should stop using the product immediately.
H-E-B recalled 300,000 units of inControl Sterile Alcohol Pads on July 7, 2025. The recall follows reports that isopropyl alcohol levels fall below the labeled concentration. Consumers should stop using the product immediately.
Evergreen Orchard Farm recalled 78 cases of grape juice on July 3, 2025, due to a lack of pasteurization and sanitation records. The recall affects products distributed in Pennsylvania, New Jersey, and New York. Consumers should not consume the product and seek refunds.
Evergreen Orchard Farm recalled 197 cases of Jujube Juice on July 3, 2025, due to lack of pasteurization and sanitation records. The juice was distributed in Pennsylvania, New Jersey, and New York. Consumers should not consume the product and seek refunds immediately.