BEUDAMED
    4 results · 35ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Recall ×

    a. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR 7X7 (5/PK) 9CENCO Catalog #68751510104. b. TIDI PRODUCTS, LLC AquaGuard DRESSING, AQUA GUARD MOISTR BARR 10X12 (5/BX) Catalog #68751510105

    FDA Recall
    Open, Classified ·Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233·Product code FRO·May 25, 2022

    Posey Connected Twice-As-Tough Cuffs

    FDA Recall
    Terminated ·TIDI PRODUCTS·Product code FMQ·April 12, 2019

    Zero-Gravity Radiation Protection System Radiology Personnel protective shield.

    FDA Recall
    Terminated ·Contour Fabricators Inc·Product code EAJ·September 9, 2016

    Widex BABY hearing aid (referred to as BABY440), powered by zinc-air batteries size 10 Intended use: BABY440 is intended for, but not limited to, babies (0 to 3 years of age) to be used as air conduction amplification devices in everyday listening environments.

    FDA Recall
    Terminated ·Widex A/S Nymollevej 6 Lynge Denmark·Product code ESD·August 31, 2018