Health & Personal Care Recalls

Baxter Healthcare CLEARLINK CONTIN-FLO IV Infusion Sets Recalled for Leaks (106,176 Units)

ImaCor ClariTEE Miniaturized TEE Probe CLT-010 Recalled Over Reversed Articulation Risk (2025)

Production assembly error resulting in the potential for reversed articulation, where moving the lever forward caused the probe tip to anteflex rather than retroflex, and vice versa.

Baxter CLEARLINK Paclitaxel IV Set Recalled for Leak Hazard in 2025 (27,072 Units)

Baxter Healthcare Recalls 49,200 CONTINU-FLO IV Solution Sets for Leakage Risk (2025)

Baxter Healthcare recalls 49,200 CONTINU-FLO IV Solution Sets distributed nationwide in the United States. IV sets may leak. Healthcare facilities and patients should stop using the device immediately and follow Baxter's recall instructions.

ConvaTec DuoDERM Extra Thin Dressings Recalled in 2025 for Foreign Matter

Wound dressing may have foreign matter on the product.

Ascend Laboratories Recalls ARIPIPRAZOLE 10 mg Tablets Over Superpotent Drug Risks (2025)

Granules Pharmaceuticals Recall: 11,928 Bottles of Dextroamphetamine Mixed Salts Suspended for Impur

Granules Pharmaceuticals Dextroamphetamine Mixed Salts ER Capsules Recall 11,909 Bottles (2025)

Granules Pharmaceuticals Recalls 3,384 Bottles of Dextroamphetamine ER Capsules for Impurity Issues

Granules Pharmaceuticals Amphetamine Capsules Recalled for Impurities Degradation Standards (2025)

Boston Scientific Extractor Pro RX Balloon Catheter Recalled Over Labeling Error (2025)

The product in incorrectly labeled. The label indicates that the skive hole should be above the balloon, while it is actually positioned below, and vice versa.

Granules Pharmaceuticals Amphetamine Salts Recall Over Impurities Degradation Specifications (2025)

Siemens Medical Solutions USA BIOGRAPH One MRI System Recalled for Helium Leak Risk (1 Unit, 2025)

Siemens MAGNETOM Skyra fit MRI Recalled for Ice Blockage Risk in 30 Units (2025)

Siemens MAGNETOM Connectom.X MRI Recalled Globally Over Ice Blockage in Vent System

Siemens Medical MAGNETOM Vida Fit MRI Recall: 27 Units at Risk of Helium Leak

Siemens MAGNETOM Skyra MRI System Recall Covers 182 Units Over Ice Blockage Risk

Siemens MAGNETOM Spectra MRI Recalled, Ice Blockage in Venting May Cause Helium Leak (2025)

Siemens MAGNETOM Verio MRI Recalled Globally Over Ice Blockage Risk in Venting System

Siemens MAGNETOM Lumina MRI System Recall Covers 71 Units Worldwide for Ice Blockage Risk

Siemens Medical Solutions USA recalled 71 MAGNETOM Lumina MRI systems worldwide, including US and 50+ countries, due to ice blockage in the magnet venting system that could cause a helium leak during a quench.