Trividia recommends that device users who receive an E-5 error code and are experiencing symptoms of high glucose should seek medical care immediately??
Trividia recommends that device users who receive an E-5 error code and are experiencing symptoms of high glucose should seek medical care immediately??
Medline updates use instructions for Electronic Homecare Beds due to risk of electrical fires and entrapment.
AirLife is removing Broselow Rainbow Tapes due to incorrectly printed medication dosing information.
MedTech/CERENOVUS is removing CEREPAK Detachable Coil Systems due to a higher than expected failure to detach rate
Certain Abbott Diabetes Care Continuous Glucose Monitor sensors may incorrect or lower than actual glucose readings
The differential pressure sensor in certain Impella devices may malfunction and cause sensor values to drift.
Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.
Integra is removing all MediHoney Wound and Burn products and certain lots of CVS Wound Gel that may have breached sterile barriers
Medline is removing certain anesthesia circuit kits due to cracks and leaks in the tubing.
Draeger is removing certain Vapor 2000 and Vapor 3000 Vaporizers due to impurities found within a component.
AirLife is removing Broselow Rainbow Tapes due to incorrectly printed medication dosing information.
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...
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...
AVID is removing bags from Organ Recovery and Medical Convenience Kits due to the bags being made of non-medical grade Poly and lacking intact seals.
[Phoenix, Arizona] - [12/22/25] - Modern Warrior is voluntarily recalling all lots of Modern Warrior Ready, a dietary supplement sold directly to consumers, after regulatory testing identified the presence of undeclared ingredients, including tianeptine, 1,4-DMAA, and aniracetam..Tianeptine can...
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
Some Ivenix LVP Primary Administration Sets were assembled with the drip chamber and Luer Lock components in reversed positions, potentially leading to clinical complications
This communication is part of the Communications Pilot to Enhance the Medical Device Recall Program
Alcon recalls Custom Pak Ophthalmic Procedure Packs due to incomplete seals that may compromise sterility. Check lot numbers, recall instructions.?