Health & Personal Care Recalls

Medline Recalls Homecare Beds Over Fire Hazard

Beckman Coulter Recalls UniCel Dxl 600 Analyzers Over Restart Issue

Beckman Coulter recalled 1,272 UniCel Dxl 600 analyzers on November 26, 2025. A communication issue may prevent the devices from restarting after shutdown, delaying test results. The recall affects multiple countries worldwide.

Medline Recalls IV Administration Sets Over Hazardous Check Valves

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Cook Medical Recalls Transjugular Liver Access Set Over Hazardous Manufacturing

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

Taro Pharmaceuticals Recalls Clindamycin Phosphate Over Impurities

Taro Pharmaceuticals recalled Clindamycin Phosphate USP, 1% topical solution on November 26, 2025. The recall affects specific lots due to failed impurity testing. Consumers should stop using the product immediately and consult healthcare providers.

Medline Recalls IV Administration Sets Due to Valve Issues

Medline Industries recalled 5,314 IV Administration Sets on November 26, 2025. The recall affects several product SKUs due to potential failure of check valve components. Patients and healthcare providers should stop using these devices immediately.

Medline Recalls IV Administration Sets Over High Hazard Risk

Medline Industries recalled 338 IV Administration Sets on November 26, 2025. The recall stems from complaints about malfunctioning check valve components. Patients and healthcare providers must stop using these devices immediately.

Medline Recalls IV Administration Sets Over Stuck Valve Hazard

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Medline Recalls IV Administration Sets Due to Sticking Valves

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Medline Recalls IV Administration Sets Due to Valve Issues

Medline Industries recalled 3,045 IV administration kits on November 26, 2025. The recall affects several Medline kits due to potential malfunction of check valve components. Patients and healthcare providers should stop using these devices immediately.

Medline Recalls IV Administration Sets Due to Valve Failure Risk

Medline Industries recalled 1,725 IV Administration Sets on November 26, 2025. The recall affects multiple kits due to potential valve malfunctions. Consumers and healthcare providers must stop using these devices immediately.

Medline Recalls IV Administration Sets Over Valve Malfunction Risk

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Medline Recalls IV Administration Sets Due to Valve Malfunction

Medline Industries recalled 12 IV administration kits on November 26, 2025. The kits may contain defective check valve components that can become stuck. Patients and healthcare providers should stop using these devices immediately.

Medline Recalls IV Administration Sets Due to Valve Malfunction

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Medline Recalls IV Administration Sets Due to Valve Issues

Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.

Winder Laboratories Recalls Morphine Sulfate Oral Solution Over Labeling Error

Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.

Cook Medical Recalls Transjugular Intrahepatic Access Sets Over Manufacturing Defects

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

Medline Recalls Electric Homecare Beds Due to Fire Hazard

Medline Industries recalled 15,581 electric homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant may overheat, posing a risk of fire in rare cases. The recall follows 58 complaints of sparking or burning from the pendant.

Medline Recalls Homecare Beds Over Fire Hazard Risk

Medline Recalls Homecare Beds Over Fire Risk from Hand Control