workplace Recalls

3M Scotch TL909-50 Thermal Laminator Recalled for Overheating

Mindray Sevoflurane V90 Vaporizer Recalled for Leakage Risk in A9 System (148 Units)

Mindray DS USA recalled 148 Sevoflurane V90 electronic vaporizers used with the A9 Anesthesia System. The devices have a potential for anesthesia leakage. Healthcare facilities should stop using the device immediately and follow manufacturer instructions.

Mindray DS USA Recalls 54 Isoflurane V90 Vaporizers for A9 Anesthesia System Over Leakage Risk (2025

M.C.I. Foods Recalls 1,040 Cases of Ready-to-Eat Egg & Cheese Breakfast Burritos and Wraps (2025)

Cooked egg ingredient for Ready-to-Eat products tested positive for Listeria Monocytogenes

Camber Ketorolac Tromethamine Injection Recall 2025 for Glass Particulates

Presence of Particulate Matter: Particulate matter identified as glass

BD Recalls 177 BACTEC Blood Culture System Units Over Unauthorized Access Risk (2025)

Beckman Coulter Recalls 160 DxC 500i Modules and DxI 9000 Analyzers in 2025 Recall

Ascend Laboratories Recalls Atorvastatin Calcium 80 mg Tablets (90-Count & 500-Count) for Failed Dil

Black Sheep Egg Company Recalls 23,400 Dozen Free Range Grade AA Eggs Over Salmonella Risk (2025)

Beckman Coulter Recalls 571 DxI 9000 Immunoassay Analyzers and DxC 500i (2025)

Cardinal Health Salem Sump PVC Tubes Recalled for ARV Breakage Risk (2025)

Cardinal Health 200, LLC recalled Salem Sump PVC Tubes worldwide after ARV breakage complaints. The anti-reflux valve can break under excessive force during use. Clinicians and patients should stop using the device and await recall instructions.

Cardinal Health Salem Sump Stomach Tubes Recalled for ARV Breakage Risk (2025)

Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214.

GE Medical Systems LOGIQ P9 R4.5 Ultrasound System Recalled for Inaccurate Liver Readings (37 Units)

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

Fisher & Paykel Recall 51,144 Airvo 2 and myAirvo 2 Humidifiers Over Power-Disconnect Audible Alert

B. Braun Medical Recalls 5,770 PERIFIX FX Epidural Anesthesia Trays for Lid Position Issue

Potential for the lid of the catheter connector to be in the incorrect position.

GE Medical Systems LOGIQ P10 Ultrasound Systems Recalled for 65 Units in 2025 Over UGAP Data Errors

The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care.

Alcon CONSTELLATION Ultravit 10K & HyperVit 20K Recall for 28,323 Units (2025)

GE HealthCare Millenium MPR Gamma Camera Recalled for 292 Units Worldwide in 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

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