Browse through 2,852 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.
Everpress Juice recalled its DETOX GREENS product on July 24, 2025, due to potential contamination with pathogenic bacteria. Consumers in 20 states should not consume the product. No injuries have been reported, but the health risk is significant.
Everpress Juice recalled cashew coffee milk on July 24, 2025, due to potential contamination with pathogenic bacteria. The product poses a high risk to consumers' health. Distribution included multiple states across the U.S.
Beckman Coulter recalled 685 boxes of MicroScan Neg MIC 56 panels distributed nationwide to U.S. healthcare facilities after contamination was reported in wells. Contamination could lead to unreliable antimicrobial susceptibility and organism-identification results. Health care providers should stop using the panels and follow Beckman Coulter recall instructions immediately.
Everpress Juice recalled Pineapple Mint Juice on July 24, 2025, due to potential contamination with pathogenic bacteria. This under-processed product poses a serious health risk to consumers. The recall affects multiple states including California and Texas.
Everpress Juice recalled its Sweet Greens product on July 24, 2025, due to possible pathogenic bacteria. The under-processed juice poses a high risk to human health. The recall affects distribution in multiple states, including California and Texas.
Everpress Juice recalled its upbeat product on July 24, 2025, due to under-processing potentially exposing consumers to pathogenic bacteria. The recall affects consumers across 15 states, including California and Texas. No injuries or illnesses have been reported, but the risk remains high.
Everpress Juice recalled spicy lemonade on July 24, 2025, due to under-processing that may lead to harmful bacteria. This recall affects consumers in 14 states including California and Texas. The product poses a high health risk and should not be consumed.
Everpress Juice recalled its cashew milk on July 24, 2025, due to under-processing that may lead to pathogenic bacteria contamination. The recall affects consumers in 15 states, posing a high health risk. Consumers should stop using the product immediately and seek a refund or replacement.
Taizhou Kangping Medical recalled 3.85 million cartons of BZK Antiseptic Towelettes on July 22, 2025. The recall stems from a lack of assurance of sterility, posing a high risk to users. Consumers and healthcare providers must stop using these towelettes immediately.
Middlefield Original Cheese Co-op recalled 246.5 pounds of 100% Grass-Fed Pepper Jack Cheese on July 21, 2025. The cheese may be contaminated with Listeria monocytogenes, which can cause serious illness. Consumers should not eat this product and seek a refund.
Merck Sharp & Dohme LLC recalled 51,320 cartons of Belsomra (suvorexant) tablets on July 21, 2025. The recall stems from a failure in dissolution specifications that could delay drug release. Consumers should stop using the product immediately and consult healthcare providers for guidance.
Bestway, Intex, and Polygroup recalled certain above-ground pools due to a drowning hazard. Nine deaths have been reported linked to this issue. The recall affects about five million pools sold since 2002.
Ascend Laboratories recalled 8,568 bottles of Amlodipine and Olmesartan Medoxomil Tablets on July 21, 2025. The recall follows reports of low dissolution results, impacting the drug's effectiveness. Consumers should stop using the product and seek guidance immediately.
Middlefield Original Cheese Cooperative recalled 640 pounds of cheese on July 21, 2025. The recall affects Monterey Jack and Farmers Cheese due to potential Listeria monocytogenes contamination. The products were distributed in Kentucky, Ohio, and Pennsylvania.
AUM Pharmaceuticals recalled 50,000 cartons of Quick Touch Alcohol Prep Pads on July 21, 2025, due to cGMP deviations. The recall affects sterile pads containing 70% isopropyl alcohol. Consumers should stop using the product immediately and contact the manufacturer.
Summa Therapeutics recalled 22 units of the Finesse BTK Multicath Injectable Angioplasty Balloon Catheter sold to healthcare facilities in New Jersey and Florida. The balloon may not meet burst specifications, raising risk during angioplasty. Healthcare providers must stop using the device immediately and follow recall instructions from Summa Therapeutics.
DJO Surgical recalled 439 AltiVate Reverse Glenoid Trays on July 18, 2025, due to potential reamer malfunction. The reamer may kick or bind during use, posing a serious risk to patients. Healthcare providers should stop using the device immediately and follow the recall instructions.
DJO Surgical recalled 907 units of the Altivate Reverse Wedge Glenoid Reamer on July 18, 2025, due to a kickback risk during use. The recall affects healthcare providers and patients nationwide across 25 states. This Class II recall warns of potential binding issues that could lead to serious injury.
DJO Surgical recalled 927 units of the Altivate Reverse Wedge Glenoid Reamer Head on July 18, 2025. The recall follows reports that the device may kick or bind up during use. Healthcare providers and patients must stop using the product immediately.
DJO Surgical recalled 447 units of the Altivate Reverse Wedge Glenoid Reamer Sleeve on July 18, 2025. The recall follows reports that the device may kick or bind during use, presenting a serious hazard to patients. Healthcare providers and patients should discontinue use immediately and follow the manufacturer's instructions.