Health & Personal Care Recalls

NOXBOX NOxBOXi Nitric Oxide Delivery System Recalled for 1,667 Units in 2025

BioPro Recalls 147 Bipolar Heads Over Sterility Risk — Check Your Model Numbers

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

Draeger Atlan A350 Anesthesia Workstations Recalled for Ventilator Failures in 2025

The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

NOXBOX Recalled 1,667 NOxBOXi Nitric Oxide Delivery System Units in 2025

The unexpected internal fault / system diagnostic error to result when a rapid succession of button selections is made to the user interface without waiting for the device to respond to user prompts.

BioPro Endo Head Ceramic Recall Affects 147 Units Over Sterility Packaging Issue (2025)

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

BioPro Recalls 147 Metal and Ceramic Femoral Heads Over Sterility Packaging Issue

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

MedicalCommunications GmbH Recalls 474 Ashvins HEYEX 2 / HEYEX PACS Software Units (2025)

Potential that the measured value may be smaller than the actual area.

BioPro Femoral Head Hip Implant Recall 147 Units in 2025 Texas and Michigan

Potential packaging issue that could compromise the sterile barrier. Defect may result in loss of sterility of the device, presenting potential risk of infection if device is implanted.

Draeger Atlan A350XL Anesthesia Workstation Recalled for Ventilator Failure Risk (223 Units) in 25+N

The device either indicated a failure of the piston ventilator before use or suffered a failure of the mechanical ventilation during use.

Beckman Coulter MicroScan Neg Multidrug Resistant MIC 1 C32368 Recall Expands Internationally (2025)

Due to manufacturing issue (incorrectly processing) with in vitro multidrug resistant test.

Iantrek CycloPen CP-300 Cyclodialysis System Recalled for Sterile Packaging Integrity (2025)

Potential for compromised integrity of the sterile packaging.

Iantrek C-Rex UNO CRX-120 Goniotomy Instrument Recalled for Packaging Integrity Issue (2025)

Potential for compromised integrity of the sterile packaging.

Sandoz Cyclophosphamide Injection 500 mg/5 mL Recalled for Temperature Excursion During Transport

cGMP deviations: Temperature excursion during transportation.

Philips Ultrasound S5-2 Transducer Recall 2025 - 1 Unit Nationwide

To provide clarification and labelling to define the useful life of ultrasound transducers in the field.

Apotex Brimonidine/Timolol Ophthalmic Solution Recalled Over Sterility Concerns (2025)

Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns

GE Healthcare Recalls 173 CSCS MAS800 Central Station Desktops Over Reboot Risk (2025)

GE Healthcare CSCS V3 MAS800 Central Station Recalled for 2,306 Units Worldwide (2025)

Spacelabs Healthcare Recalling 8,179 DVI Display Cables Over EMI Interference Risk (2025)

Spacelabs Healthcare DVI Display Cables Recalled for EMI Risk in 2025 (012-0895-12, 820 Units)

Apotex Ketorolac Tromethamine Ophthalmic Solution Recall 2025: 493,468 Bottles Nationwide

Lack of Assurance of Sterility; atypical weight loss due to improper bottle sealing leading to potential sterility concerns