Health & Personal Care Recalls

Philips Medical Systems Recalls Allura Xper FD20 Over Electrical Hazard

Diagnostica Stago Recalls Asserachrom HPIA Kit Over False Negatives

Diagnostica Stago issued a recall for 438 Asserachrom HPIA kits on December 15, 2025. The kits, used to detect PF4 antibodies, may produce false negative results. The affected lot is 271288, distributed worldwide including multiple U.S. states.

Broselow Recall Due to Dangerous Dosing Errors in ALS Organizer

Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.

Intuitive Surgical Recalls da Vinci SP Access Port Kits Over Sterility Risk

Access Port System tray may develop cracks potentially resulting in a sterility breach.

Wilson-Cook Medical Recalls Nasal Jejunal Feeding Tube Over Missing Component

Wilson-Cook Medical recalled 60 units of Nasal Jejunal Feeding Tube NJFT-10 on December 15, 2025. The tubes were packaged without the necessary nasal transfer tube component. This defect poses a high hazard risk for patients requiring feeding assistance.

Philips Recalls Allura Xper FD20 OR Table Due to Electrical Hazard

Philips Medical Device Recalled Due to Electrical Hazard

Philips Medical Systems Recalls Allura Xper FD20 Biplane Over Electrical Hazard

Philips Medical Systems recalled 23 units of the Allura Xper FD20 Biplane on December 15, 2025. The recall affects systems with improperly installed drip trays, posing an electrical hazard. Health providers and patients must stop using the device immediately.

Philips Recalls Allura Xper FD10C Systems Over Electrical Hazard

LEASEIR Surgical Laser Recalled Over Missing Danger Label

The console label for affected devices is missing the "DANGER" symbol.

Broselow Pediatric Emergency Tape Recalled Over Dosing Errors

Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.

Philips Medical Systems Issues Recall for Allura Xper FD10/10

Philips Medical Systems Recalls Allura Xper FD20/20 Over Electrical Hazard

SunMed Recalls Broselow Pediatric Emergency Tape Over Dosing Errors

Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.

Philips Recalls Allura Xper FD20 Over Electrical Hazard

Philips recalled 79 Allura Xper FD20 systems on December 15, 2025. The recall affects systems with an improperly installed drip tray which can cause electrical short-circuits. Healthcare providers and patients must stop using the device immediately.

ICU Medical Recalls Plum Duo Infusion Pump Over High Hazard Risk

ICU Medical recalled the Plum Duo Infusion Pump on December 15, 2025, after reports of malfunctioning flush programming. The recall affects models 400020401 and 400021001 sold worldwide. This issue may pose a high risk to patient safety.

Hologic Recalls Brevera Breast Biopsy System Due to Contamination Hazard

Presence of particulates in affected devices that can be deposited into breast tissue during use.

ICU Medical IV Pump Recalled Due to Programming Error Risk

Immunotech A.S. Recalls Estrone RIA Kit Over False Results Hazard

Immunotech A.S. recalled 160 Estrone RIA kits on December 15, 2025, due to a risk of falsely high patient results. This class II recall affects kits distributed in multiple countries, including the US and several European nations.

Philips Medical Systems Recalling Allura Xper FD10 Over Electrical Risk