electronic Recalls

GE Healthcare Recalls 82 Millenium Myosight Dual-Head Gamma Cameras for Cardiac Imaging (2025)

Argon Medical Devices Recalls 1,821 Option Elite IVC Filters for Dilator Resistance Risk (2025)

Due to complaints of increased resistance when advancing the dilator within the introducer sheath. This issue could potential result in procedural delays and/or risk of venous intimal injuries if excessive force is applied

UIH Technologies uEXPLORER MD PET/CT Recall for 2 Units in 2025

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

GE HealthCare Optima NX Recall for Detector Fall Risk (1 Unit)

Shanghai United Imaging Healthcare CT X-ray System uCT 550 MD Recall for 22 Units in 2025

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

UIH Technologies Recalls 8 Shanghai United Imaging uCT 530 MD CT Scanners Over Interference Risk (24

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

UIH Technologies uMI 550 MD PET/CT Recalled for 95 Units Over Mechanical Interference Risk (2025)

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

UIH Technologies uCT 780 MD CT Scanner Recalled for Cover Interference (2025)

Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement.

Olympus BF-P190 Bronchoscope Recall Updated for 2025 IFU Guidance

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus BF-H190 Bronchovideoscope Recall Expanded for IFU Updates in 2025

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus EVIS EXERA II BF-1T180 Bronchovideoscope Recall for IFU Update — 5,247 Units (2025)

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus BF-H1100 Bronchovideoscope Recall 1,867 Units Overseas in 2025

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus EVIS EXERA III BF-1TH190 Bronchoscope Recall 8,587 Units in 2025

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Olympus EVIS EXERA III BF-Q190 Bronchovideoscope Recall Expands in 2025 for IFU Updates

Additional IFU updates to provide further clarification on safe and effective use of bronchoscopes when used in conjunction with laser, argon plasma coagulation, and high-frequency therapy equipment.

Ferno Power X2 Powered Ambulance Cot Recalled for 138 Units Nationwide in 2025

Ferno-Washington Inc. recalled 138 Power X2 powered ambulance cots nationwide. The recall is due to fastening post hardware that could loosen and detach. Stop using the device and contact Ferno-Washington for instructions.

Boston Scientific TENACIO Pump Recall 2025 for Inflation Deflation Issues

The potential for devices to experience inflation and/or deflation performance issues or difficulties.

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 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.

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.

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.