Early Alert: Wound and Burn Dressing Issue from Integra LifeSciences
Integra is removing all MediHoney Wound and Burn products and certain lots of CVS Wound Gel that may have breached sterile barriers
Integra is removing all MediHoney Wound and Burn products and certain lots of CVS Wound Gel that may have breached sterile barriers
Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.
Medline is removing certain anesthesia circuit kits due to cracks and leaks in the tubing.
AirLife is removing Broselow Rainbow Tapes due to incorrectly printed medication dosing information.
Draeger is removing certain Vapor 2000 and Vapor 3000 Vaporizers due to impurities found within a component.
Boston Scientific is removing certain stents and delivery systems due to issues with deployment and expansion.
CENTER VALLEY, Pa., (January 16, 2026) — Olympus Corporation has announced the expansion of a previous global medical device removal action for ViziShot 2 FLEX (19G) EBUS -TBNA needles (“ViziShot 2 FLEX”) after receiving and investigating complaints of device components ejecting or detaching during
ABBOTT PARK, Ill., Nov. 24, 2025 — Abbott has initiated a medical device correction for certain FreeStyle Libre 3 and FreeStyle Libre 3 Plus sensors in the United States after internal testing determined that some sensors may provide incorrect low glucose readings.
Prismaflex Set deaeration chambers may dislodge from the Prismaflex Control Unit during use.
Rosemead, CA, ANTHONY TRINH, 123herbals LLC is voluntarily recalling all lots of Silintan capsules to the consumer level. FDA analysis has found the product to be tainted with meloxicam. Meloxicam, is an approved Nonsteroidal Anti-Inflammatory Drug, (NSAID) indicated for management of osteoarthritis
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