immediate action Recalls

Vortex Surgical Recalls Laser Probes Due to Infection Risk

Vortex Surgical recalled 14,789 laser probes on December 16, 2025, due to potential bioburden contamination. The recall affects multiple catalog numbers distributed worldwide. Healthcare providers and patients must stop using these devices immediately.

Vortex Surgical Recalls Vitrectomy Lenses Due to Infection Risk

Vortex Surgical recalled 14,789 single-use vitrectomy lenses on December 16, 2025. The recall affects models with potential seal voids that could lead to bioburden contamination. Patients and healthcare providers must stop using these devices immediately.

Alembic Pharmaceuticals Recalls Fesoterodine Tablets for Impurity Risk

Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.

Philips Recalls Allura Xper FD20 OR Table Due to Electrical Hazard

Novadoz Pharmaceuticals Recalls Glycopyrrolate Oral Solution Over Safety Concerns

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

Philips Medical Systems Recalls Allura Xper FD20 Over Electrical Hazard

Broselow Pediatric Emergency Tape Recalled Over Dosing Errors

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

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.

Philips Medical Systems Issues Recall for Allura Xper FD10/10

Broselow Recall: Harmful Dosing Errors in Pediatric Organizer

Broselow recalled 89 units of the BROSELOW FILLED BROSELOW ORGANIZER on December 15, 2025. The product contains harmful dosing errors for critical medications. Healthcare providers must stop using the device immediately.

Philips Recalls Allura Xper FD20 Biplane Over Electrical Hazard

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.

Philips Medical Systems Recalls Allura Xper FD20/10 Over Electrical Hazard

Philips Medical Systems recalled four Allura Xper FD20/10 systems on December 15, 2025. The company identified that a drip tray was not installed, posing a risk of electrical shorts. This defect could lead to system shutdowns.

Philips Recalls Allura Xper FD10F Systems Due to Electrical Hazard

Philips Recalls Allura Xper FD10C Systems Over Electrical Hazard

Philips Medical Device Recalled Due to Electrical Hazard

Philips Medical Imaging System Recalled Over 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 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.