immediate action Recalls

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

Baxter Healthcare CLEARLINK CONTIN-FLO IV Solution Sets Recalled for Leaks (2025)

Baxter Healthcare Recalls 8,368 CLEARLINK CONTINU-FLO IV Sets for Leakage Risk (2025)

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 Recalls 15,552 CLEARLINK IV Extension Sets for Leakage Risk (2025)

Baxter Healthcare recalled 15,552 CLEARLINK SYSTEM EXTENSION SETS nationwide in the United States. The IV extension sets may leak. Healthcare providers and patients should stop using the device immediately and follow Baxter recall instructions.

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.

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

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

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

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

ConvaTec DuoDERM Extra Thin Dressings Recalled in 2025 for Foreign Matter

Wound dressing may have foreign matter on the product.

Northeast Scientific NES Reprocessed 1.4mm OTW Turbo Elite Laser Atherectomy Catheter Recall 173 Un­

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

Northeast Scientific Recalled 1,019 Reprocessed Turbo Elite Atherectomy Catheters Over Sterility Bre

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

Baxter Healthcare's CLEARLINK CONTINU-FLO IV Set Recall for Leakage Risk (2025)

Baxter Healthcare Corp. recalled 12,720 CLEARLINK SYSTEM CONTINU-FLO IV sets distributed nationwide to healthcare facilities. The devices may leak during use. Hospitals and clinicians should stop using immediately and follow Baxter's recall instructions.

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.

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.

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

Northeast Scientific Recalled 561 Units of NES Reprocessed 0.9mm OTW Turbo Elite Laser Atherectomy C

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

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.

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

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

Product does not declare wheat in the allergen statement.

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

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