workplace Recalls

Siemens MAGNETOM Vida MRI Recall 237 Units Worldwide Over Ice Blockage Risk (2025)

Frontier Devices Recalls 2,700 REF 301.914S1 14 mm Distraction Pins (2025)

Labeling includes shelf life that has not been validated.

Boston Scientific Pacemakers Recalled for Safety Architecture Software Issue (41,009 Units, 2025)

Maquet Cardiovascular Heartstring III Proximal Seal System Recalled for 168 Units Worldwide (2025)

Three failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartstring Seal to provide adequate hemostasis.

Werner Recalls 20' and 24' Multi-Max Pro Ladders for Fall Hazard (2025)

Philips Ingenuity CT Brazil 728325 CT System Recalled for 3 Units in 2025

The patient support table (couch) may descend unexpectedly to the lowermost position due to a component (ball screw) misalignment after a replacement.

Fresh & Ready Foods Recalls 233 Spanish Club Ciabatta Sandwiches for Undeclared Wheat/Milk Allergens

undeclared allergen (Wheat and Milk) on ready to eat sandwiches.

Fresh & Ready Foods Piccolo Pranzo Box Recalled for Undeclared Wheat, Milk Allergens — 233 Units (RE

undeclared allergen (Wheat and Milk) on ready to eat sandwiches.

Beckman Coulter UniCel DxH 690T Hematology Analyzer Recall Over HGB Photometer (2025)

Hematology analyzers configured with HGB photometers may result in erroneously high hemoglobin (HGB) results on samples with elevated white blood cell (WBC) counts.

HEB Blueberry Yogurt Pretzels Recalled for Undeclared Wheat Allergen (2025)

Penner Patient Care Bathing Spa Devices Recall for Missing Unique Device Identifier (Z-1500-2026)

The device does not bear a unique device identifier.

Viona Pharmaceuticals Recalls Tavaborole Topical Solution 5% Over Discoloration (2025)

Baxter Continu-Flo Intravascular Set Recalled for Tubing Separation — 14,400 Units in 2025

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for one lot of Continu-Flo solution sets listed below due to customer reports of tubing separation.

Medline Medline Extremity Pack DYNJ45701B Sterile Kit Recall Affects 88 Units (2025)

Convenience kits labeled as sterile have not gone through the sterilization process.

Hi-Tech Pharmaceuticals’ PrimeNutrition PhytoForm Fruits & Greens Recall for Unapproved Drug Claims

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals Formutech Nutrition Joint Formula Recalled for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals Joint-RX Dietary Supplement Recalled for Unapproved Drug Claims (2025)

SeaSpine Orthopedics Recalled 74 Reef TA Inserter Instruments for Reef Interbody System (2025)

AVID Medical CPT BASIC IR PACK 1646381 Recall for Sterility Risk (2025)

AVID Medical recalls 228 CPT BASIC IR PACKs sold nationwide, including Florida, due to open header bag seals that may compromise sterility. The recall is active as of September 17, 2025. Consumers should stop use and follow manufacturer instructions.

Wasatch Photonics Raman Spectrometers Recall Expanded for Laser Safety Risks (2025)