immediate action Recalls

Medline Recalls Homecare Beds Over Fire Hazard

Medline Recalls Electric Homecare Beds Due to Fire Hazard

Medline Industries recalled 138,412 electric homecare beds on November 26, 2025. Hazardous hand control pendants may overheat and pose a fire risk. The recall follows 58 reports of sparking, burning, and smoking incidents.

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.

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.

Ozark Trail Tabletop 1-Burner Butane Camping Stove BG2247A1 Recalled by Walmart in 2025

Medline Recalls Homecare Beds Over Fire Hazard Risk

Medline Industries recalled 373,392 homecare beds on November 26, 2025, due to a fire hazard. The hand control pendant can overheat, causing sparking or burning. The recall affects models MDR107002E and MDR107002E-4 sold in the U.S. and Canada.

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 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 Introducer Sheaths Over Manufacturing Errors

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.

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.

Medline Recalls IV Administration Kits Over Valve Malfunction Risk

Medline Industries recalled 11,173 IV administration kits on November 26, 2025. The kits contain B. Braun IV Administration Sets and Pump Administration Sets with faulty check valves. These valves may become stuck, posing a high hazard to patients.

Beckman Coulter Recalls 6,457 Immunoassay Analyzers Over Restart Issues

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.

Prairie Farms Milk Recalled Due to Food-Grade Cleaning Agents

Prairie Farms Dairy recalled 3,752 gallons of Fat Free Milk on November 25, 2025. The milk may contain food-grade cleaning agents, posing a health risk. Consumers should not consume the product and seek refunds or replacements.

Imu-Tek Colostrum Powder Recalled Due to Undeclared Allergen

Imu-Tek Animal Health recalled 113 bottles of Immuno-5 Colostrum Powder on November 25, 2025. The product contains an undeclared milk allergen, posing a risk to consumers with milk allergies. The recall affects states including CA, TX, and FL.

Ferndale Laboratories Recalls Mastisol Liquid Adhesive Over Hazard

Ferndale Laboratories recalled 24,589 vials of Mastisol Liquid Adhesive due to a defect. The butyrate tube may crack during use, making the product unusable. The recall affects products distributed in the U.S. and the U.K., announced on November 25, 2025.

Gimme Coffee Recalls Pods Over Undeclared Caffeine Hazard

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

ICU Medical Recalls LifeShield Infusion Safety Software Due to Risk

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.