2,756 recalls tagged with “immediate action”.
Gimme Coffee, Inc. recalled 252 boxes of Decaf de Agua coffee pods on November 24, 2025. The product contains undeclared caffeine, posing a risk to consumers sensitive to caffeine. Affected products include those with best-by dates of September 30, 2025, and October 15, 2025.
Abbott Diabetes Care recalled 1,663,241 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may lead to incorrect low glucose results, creating serious health risks for users. Patients should stop using the sensors immediately and follow recall instructions.
ICU Medical recalled LifeShield Drug Library Management software on November 24, 2025. A software issue limits concentration precision to one decimal place, risking incorrect drug dosages. Users should stop using the product immediately and follow recall instructions.
Draeger, Inc. recalled 188 units of the Vapor 3000 anesthetic vaporizer on November 24, 2025. The devices contained impurities in a component not delivered within specification. Healthcare providers and patients must stop using the devices immediately.
Bell Industries recalled 66 units of Zen Cleanse Blend herbal tea on November 24, 2025. The recall follows potential Salmonella contamination. The product was distributed to three customers in Massachusetts, Texas, and Wisconsin, but did not reach retail shelves.
Draeger, Inc. recalled 431 units of the Vapor 2000 anesthetic vaporizer on November 24, 2025. A component of the devices contained impurities and did not meet specifications, posing a high hazard risk. Healthcare providers and patients should cease use immediately and follow recall instructions.
Abbott Diabetes Care recalled 258,913 FreeStyle Libre 3 Plus sensors on November 24, 2025. Manufacturing issues may lead to incorrect low glucose results, posing a high risk to users. Consumers should stop using the device immediately and follow the recall instructions.
Abbott Diabetes Care recalled 8,062 FreeStyle Libre 3 Plus sensors on November 24, 2025. A manufacturing issue may cause inaccurate low glucose readings, posing serious health risks. Consumers should stop using the device immediately and follow recall instructions.
ICU Medical recalled the LifeShield Infusion Safety Software Suite v2.2 on November 24, 2025. The software fails to operate as expected for migrated libraries, risking medication delivery errors. The recall affects seven customers across several states, including California and New York.
Breckenridge Pharmaceutical, Inc. recalled 7,389 bottles of Duloxetine Delayed-Release Capsules on November 24, 2025. The recall stems from CGMP deviations and the presence of N-nitroso-duloxetine impurity above FDA limits. Consumers should stop using the product immediately and contact healthcare providers for guidance.
Towa Pharmaceuticals recalled 3,397 bottles of Duloxetine Delayed-Release Capsules on November 24, 2025. The recall stems from CGMP deviations resulting in N-nitroso-duloxetine levels exceeding FDA limits. Consumers must stop using the product immediately.
Alcon Laboratories, Inc. recalled 151 units of Custom Pak surgical procedure packs on November 24, 2025. The recall stems from incomplete seals that may affect sterility. Healthcare providers and patients should stop using the products immediately.
Abbott Diabetes Care recalled over 1 million FreeStyle Libre 3 sensors on November 24, 2025, due to a manufacturing issue. The defect may lead to incorrect low glucose readings, posing a serious health risk. Affected sensors were distributed across the U.S. and several international markets.
Changchun Wancheng Bio-Electron Co. recalled 32,500 Keto-pH-Uric Acid Test Strips on November 22, 2025. The strips may provide inaccurate results and lead to inappropriate medical intervention. The recall affects products distributed nationwide in Texas, Georgia, and California.
LotFancy recalled 91,366 urinary tract infection test strips on November 22, 2025. The strips may produce false results, risking inappropriate medical intervention. Affected products include various models sold nationwide in states like Texas, Georgia, and California.
Changchun Wancheng Bio-Electron Co. recalled 1,000 LH One Step Ovulation Test Devices on November 22, 2025. The tests may deliver false or inaccurate results, potentially leading to inappropriate medical intervention. The recall affects U.S. consumers in Texas, Georgia, and California.
GBC Food Services recalled EverRoast Chicken Caesar Salad on November 22, 2025, due to potential Listeria monocytogenes contamination. The recall affects 2 units of the product distributed in Kentucky and Indiana. Consumers should not consume this product and seek a refund or replacement.
Changchun Wancheng Bio-Electron Co. recalled 500 Vivoo pH Test strips on November 22, 2025. The recall follows concerns over false diagnostic results that could lead to inappropriate medical interventions. These devices were distributed nationwide, including Texas, Georgia, and California.
Vivoo recalled 3,000 vaginal pH tests on November 22, 2025. The tests may cause false results leading to inappropriate medical interventions. The products were distributed nationwide, including Texas, Georgia, and California.
GBC Food Services recalled 11 units of EverRoast Chicken Caesar Wrap on November 22, 2025. The recall occurred due to potential contamination with Listeria monocytogenes. The affected products were distributed in Kentucky and Indiana.