stop use immediately Recalls

Baxter Healthcare Recalled 473,040 CLEARLINK IV Solution Sets for Leakage Risk (2025)

Baxter Healthcare CLEARLINK CONTINU-FLO IV Set Recalled for Leaks in 2025 (958,351 Units)

Baxter Healthcare Recalls 18,720 CLEARLINK Non-DEHP IV Sets for Leakage Risk (2025)

Northeast Scientific Laser Atherectomy Catheter Recalled for Sterile Barrier Breach Risk (2025)

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

Getinge 88-Series Washer-Disinfector 88-5 Recalled for Overheat Risk in 788 Units (2025)

Potential for device to overheat during operation f the circulation pressure calibration was not performed or had been performed incorrectly, and the low-pressure alarm is not triggered.

ConvaTec DuoDERM Extra Thin Dressings Recalled in 2025 for Foreign Matter

Wound dressing may have foreign matter on the product.

Baxter Healthcare Recalls 136,512 CLEARLINK IV Sets DUO-VENT for Leak Risk (2025)

Tas Tematic Foods Frozen Shrimp IQF 2-lb Bags Recalled for Nitrofuran Contamination (2025)

Product which was on FDA hold for high levels of Nitrofuran was inadvertently distributed.

Northeast Scientific NES Turbo Elite Laser Atherectomy Catheter Recall: 199 Units (2025)

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

Baxter Healthcare Recalled 69,936 CLEARLINK IV Extension Sets for Leak Risk (2025)

Baxter Healthcare recalled 69,936 CLEARLINK System Non_DEHP Extension Sets sold nationwide to hospitals and clinics. The IV extension sets may leak. Healthcare providers should stop using the device and follow Baxter's recall instructions.

Herbal Creations Colostrum Powder Recall for Milk Allergen Labeling Error (2025)

Bulk packaged dietary ingredient manufacturer product label does not declare Milk as an allergen ingredient.

Fresenius Medical Care Optiflux Dialyzers Recalled for Press-On Cap Issue (172,494,732 units, 2025)

To provide further information to the user to ensure proper use of the medical device. the caps had been changed from a threaded version to a press-on version whereby the user must press the caps firmly onto the dialyzer to securely affix the cap.

Northeast Scientific NES Reprocessed 2.0mm RX Turbo Elite Laser Atherectomy Catheter Recall 2026

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

NES Reprocessed 1.7mm RX Turbo Elite Laser Atherectomy Catheter Recall: 616 Units In US Distribution

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

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.

Rolling Pin Baking Company Recalls 127,680 Dubai Style Chocolate Pouches for Undeclared Wheat (2025)

Product does not declare wheat in the allergen statement.

Baxter recalls 2,304 CLEARLINK IV Extension Sets for leak risk in 2025

Northeast Scientific NES Reprocessed 0.9mm Turbo Elite Laser Atherectomy Catheter Recall 2025

Potential for breaches in the sterile barrier packaging, compromising sterility assurance.

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.