164 recalls tagged with “workplace”.
Siemens Medical Solutions USA recalled 237 MAGNETOM Vida MRI scanners sold worldwide to healthcare providers. The recall cites ice forming in the magnet venting system. A quench could lead to a helium leak into the scanning room. Hospitals must stop using the devices and await manufacturer instructions.
Frontier Devices recalled 2,700 units of REF 301.914S1 14 mm Distraction Pin sold nationwide by multiple retailers. The labeling includes shelf life that has not been validated. Healthcare providers and patients should stop using this device immediately and follow the manufacturer’s recall instructions.
Boston Scientific recalled 41,009 pacemakers worldwide after a software flaw could prevent Safety Mode activation. The defect affects devices in the ACCOLADE family and several related models. Patients and healthcare providers should stop using the device immediately and follow recall instructions from the manufacturer.
Maquet Cardiovascular recalled 168 Heartstring III Proximal Seal System intravascular occluders worldwide, including the United States. Three failure modes have been identified: loading the Heartstring Seal, deploying it into the aortotomy, and achieving adequate hemostasis. Healthcare facilities should stop using the device and follow the manufacturer’s recall instructions.
Werner recalls 2 ladder models sold nationwide after reports of locking mechanism jams. The recall affects Werner 20' ALMP-20IAA and 24' ALMP-24IAA Multi-Max Pro multi-purpose ladders. Consumers should stop using these ladders and contact Werner for a full refund.
Beckman Coulter recalled the UniCel DxH 690T COULTER Cellular Analysis System configured with the LED HGB Photometer REF C34520. The hematology analyzer may produce erroneously high hemoglobin results on samples with elevated white blood cell counts. Labs should stop using the device immediately and follow Beckman Coulter's recall instructions.
Fresh & Ready Foods recalled 233 Piccolo Pranzo Box sandwiches after undeclared wheat and milk allergens were detected. The product was distributed to 15 California locations. Consumers should not eat the product and should contact Fresh & Ready Foods for refund or replacement information via email.
Fresh & Ready Foods recalled 233 Spanish Club Ciabatta sandwiches sold to 15 California locations after discovering undeclared wheat and milk allergens. The recall is Class I and the hazard is an undisclosed allergen on ready-to-eat sandwiches. Consumers should not eat the sandwiches and should contact Fresh & Ready Foods for refunds or replacements by email.
Philips recalled 3 Ingenuity CT Family Brazil systems, Model 728325, distributed worldwide, including the United States. A ball screw misalignment after a replacement may cause the patient support table to descend to the lowest position. Hospitals and clinicians should stop using the device and follow Philips recall instructions.
HEB recalled 468 cases of 8oz Blueberry Flavored Yogurt Pretzels distributed in Texas by Dollins Pecan Co, Inc. The product contains undeclared wheat allergen. Consumers should not eat the product and should contact Dollins Pecan Co, Inc via email for refund or replacement.
Penner Patient Care recalled 643 devices nationwide after the FDA flagged missing unique device identifiers. The recall affects a broad range of Penner Pacific Bathing Spa models. The device lacks a unique device identifier, posing regulatory and traceability concerns. Stop using the device and follow recall instructions from Penner Patient Care or a healthcare provider.
Viona Pharmaceuticals recalls Tavaborole Topical Solution 5% 10 mL bottles, distributed nationwide in the U.S. The effective recall date is August 12, 2025. The product is manufactured by Zydus Lifesciences Ltd. Discoloration was cited as the reason for the recall. Consumers should stop using the product and contact the distributor for guidance.
Baxter Healthcare Corporation issued an urgent medical device recall for one lot of Continu-Flo intravascular solution sets, 14,400 units distributed nationwide in the United States. Customer reports indicate tubing separation. Health care providers and patients should stop using the device immediately and follow recall instructions.
Medline Industries recalled 88 units of the Sterile Extremity Pack DYNJ45701B after finding that kits labeled as sterile had not undergone sterilization. The affected distribution covered Florida, Maryland, New Jersey and Tennessee. Hospitals and clinics should stop using the kit immediately and follow Medline's recall instructions.
SeaSpine Orthopedics recalled 74 Reef TA Inserter instruments used with the Reef Interbody System, distributed worldwide to hospitals and surgical centers. The inserter may cause difficulty disengaging the implant or improper positioning, prolonging surgery and possibly requiring intraoperative revision. Hospitals and surgeons should stop using the device and follow recall instructions from SeaSpn
Hi-Tech Pharmaceuticals recalled 85,950 units of PrimeNutrition PhytoForm Fruits & Greens Formula after FDA enforcement flagged unapproved drug claims and misbranding. The dietary supplement was distributed to 40+ states before the recall was issued on 2025-08-06 and remains active. Consumers should not consume the product and should seek refund or replacement from Hi-Tech Pharmaceuticals.
Hi-Tech Pharmaceuticals recalled 85,950 units of Formutech Nutrition Flexible Joint Formula with Cissus Quadrangularis sold nationwide after regulators flagged unapproved drug claims. The product claims to support tendons and muscles and promote healthy cartilage, which regulators say is not approved. Consumers who purchased the supplement should not use it and should await refund or replacement,'
Hi-Tech Pharmaceuticals recalled Joint-RX, a 600 mcg dietary supplement sold nationwide, after regulators flagged unapproved drug claims. The recall affects 85,950 units shipped to more than 40 states. Consumers should stop using the product and contact the company for refunds or replacements.
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 recalled 192 Raman spectrometers in the United States after identifying two potential laser safety failure modes. Models 785-SR-ILP, 785-SR-ILC, 830-SR-ILP, 830-SR-ILC, and 785-ER-ILC are included. The defect could occur under excessive force or extreme continuous vibration. Stop using immediately and follow the manufacturer’s recall instructions.