immediate action Recalls

Bell Industries Recalls Zen Cleanse Blend Tea for Salmonella Risk

Draeger Vapor 2000 Anesthetic Vaporizer Recalled Over Impurities

A certain component of affected devices was not delivered within specification and contained impurities.

Abbott Recalls FreeStyle Libre 3 Plus Sensors Due to Hazardous Readings

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Abbott Recalls FreeStyle Libre 3 Plus Sensor Over Glucose Errors

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

ICU Medical Recalls LifeShield Infusion Software Over Delivery Risk

Breckenridge Recalls Duloxetine Capsules Over Chemical Hazard

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit

Alcon Laboratories Recalls Custom Pak Surgical Packs Over Sterility Issues

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 Recalls FreeStyle Libre 3 Sensor Over Glucose Reading Errors

Due to a manufacturing process issue that may cause carbon build up in the sensor that may result in incorrect low glucose results

Duloxetine Capsules Recalled Over High N-Nitroso Impurity Risk

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.

Changchun Wancheng Recalls Ovulation Test Over False Results Risk

LotFancy Urinary Tract Infection Test Strips Recalled for False Results

Dr. Anna Cabeca Test Strips Recalled Over False Diagnostic Risks

GBC Food Services Recalls Chicken Caesar Salad Over Listeria Risk

Potential presence of Listeria monocytogenes.

Changchun Wancheng Bio-Electron Recalls Vivoo pH Test for Inaccurate Results

Vivoo Vaginal pH Test Recalled Over Inaccurate Results Risk

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 Recalls Chicken Caesar Wrap for Listeria Risk

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.

Vivoo Test Strips Recalled Due to False Diagnostic Risk

Changchun Wancheng Bio-Electron Co. recalled 3,300 Vivoo test strips on November 22, 2025. The devices may provide inaccurate results, leading to inappropriate medical actions. Affected products include sodium, Vitamin C, and hydration tests.

Changchun Wancheng Recalls Male Fertility Test Over Inaccurate Results

Changchun Wancheng Recalls Male Fertility Test Over False Results

Changchun Wancheng Bio-Electron Co. recalled 1,000 male fertility sperm tests on November 22, 2025. The tests were distributed without proper FDA clearance and may yield inaccurate results. This could lead to inappropriate medical interventions by users.

Wegmans Grated Cheese Recalled Over Listeria Contamination

Wegmans Food Markets recalled 2,773.9 pounds of grated cheese on November 22, 2025. The product may be contaminated with Listeria monocytogenes, which poses serious health risks. Consumers should not consume the product and seek refunds immediately.