cpsc regulated Recalls

ICU Medical Recalls LifeShield Infusion Safety Software Due to Risk

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

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

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 Over Low Glucose Risk

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

Breckenridge Recalls Duloxetine Capsules Over Chemical Hazard

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

Draeger Vapor 3000 Anesthetic Vaporizer Recalled Due to Impurities

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.

ICU Medical Recalls LifeShield Infusion Software Over Delivery Risk

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.

Gimme Coffee Recalls Pods Over Undeclared Caffeine Hazard

Changchun Wancheng Bio-Electron Recalls Diagnostic Test Strips

Changchun Wancheng Bio-Electron Co. recalled 1,000 units of S. Typhi/Para Typhi A Antigen test strips on November 22, 2025. The recall affects tests distributed nationwide, which may produce false results and lead to inappropriate medical intervention.

Changchun Wancheng Recalls Ovulation Test Over False Results Risk

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.

Changchun Wancheng Recalls Male Fertility Test Over Inaccurate Results

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

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 Bio-Electron Recalls Vivoo Protein Test Over False 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.

Dr. Anna Cabeca Test Strips Recalled Over False Diagnostic Risks