BEUDAMED
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    ZIP 16 SURGICAL SKIN CLOSURE DEVICE (PART#: PS1160, LOT/SERIAL#: UNKNOWN)

    FDA Adverse Event
    Injury ·STRYKER / STRYKER INSTRUMENTS·Product code KGX·February 4, 2021

    PKG, 1688 AIM 4K CAMERA HEAD, C-MOUNT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·July 20, 2023

    WAYNE PNEUMOTHORAX SET

    FDA Adverse Event
    Injury ·COOK, INC.·Product code DQR·May 7, 2014

    PKG, 1688 AIM 4K CAMERA HEAD, C-MOUNT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·December 13, 2023

    PKG, 1488 HD 3-CHIP CAMERA HEAD, C-MOUNT

    FDA Adverse Event
    Malfunction ·STRYKER ENDOSCOPY-SAN JOSE·Product code GCJ·February 9, 2023

    VALVEGATE SUTURE CATCHER

    FDA Adverse Event
    Malfunction ·GEISTER MEDIZINTECHNIK GMBH·Product code DTH·December 19, 2014

    SPRINT QUATTRO SECURE S MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code LWS·May 2, 2025

    2-0 TUCNOW 3303-56

    FDA Adverse Event
    Other ·US SURGICAL·Product code DTH·May 16, 2000

    GORE-TEX SUTURE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code DTH·May 11, 1999

    VALVEGATE

    FDA Adverse Event
    Malfunction ·GEISTER MEDIZINTECHNIK GMBH·Product code DTH·January 17, 2014

    GORE-TEX SUTURE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code DTH·March 25, 2003

    GORE-TEX SUTURE CV5

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DTH·April 30, 2009

    GORE-TEX SUTURE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOC., INC.·Product code DTH·August 8, 1997

    GORE-TEX SUTURE

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES,INC·Product code DTH·December 15, 1999

    PROLENE BLUE MONOFILAMENT

    FDA Adverse Event
    Malfunction ·ETHICON·Product code DTH·October 14, 2004

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code DTH·August 24, 1999

    VALVEGATE

    FDA Adverse Event
    Malfunction ·GEISTER SURGICAL INSTRUMENTS·Product code DTH·December 19, 2013

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·September 18, 2017

    UNK HYLAMER LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JDI·October 29, 1999

    SAFE GAIT ACTIVE 360 DYNAMIC MOBILITY TRAINER

    FDA Adverse Event
    Malfunction ·DIH TECHNOLOGIES INC.·Product code BXB·May 30, 2024