BEUDAMED
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    QUICK COUPLING FOR PINS Ø3.2MM

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code GEY·January 28, 2014

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code GEY·December 16, 2013

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·January 6, 2015

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code GEY·January 28, 2014

    BATTERY REAMER/DRILL II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·July 10, 2014

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code GEY·December 9, 2013

    BATTERY REAMER/DRILL

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code MOQ·June 5, 2014

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·September 16, 2014

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·September 30, 2014

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·July 10, 2014

    BATTERY OSCILLATOR II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code GEY·September 23, 2014

    POWER MODULE FOR TRAUMA RECON SYSTEM

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES PRODUCTS LLC·Product code MOQ·August 28, 2019

    Battery Power Line II Battery Oscillator, DePuy Synthes Power Tools, The Anspach Effort Inc.

    FDA Recall
    Terminated ·The Anspach Effort, Inc.·Product code MOQ·November 25, 2015

    KLS Martin Battery Pack, REF: KLS BP2 001, and KLS BP2 040 (bulk case of 40), used in conjunction with the KLS Martin MaxDriver 2.0 surgical driver, REF: KLS-SD-2000

    FDA Recall
    Open, Classified ·Pro-Dex Inc·Product code MOQ·September 23, 2024

    DermaStyle Chroma 2-blue and red light device indicated to be used in treating skin blemishes; portable home therapy; Lumiport LLC.

    FDA Recall
    Terminated ·Lumiport, LLC·Product code MOQ·September 28, 2006

    Battery Pack KLS-SD-1000 Case (40 ct) Models: KLS-BP-040 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).

    FDA Recall
    Terminated ·Pro-Dex Inc·Product code MOQ·December 23, 2015

    Battery Pack KLS-SD-1000 Single Models: KLS-BP-001 Used to power the KLS Martin Max Driver (battery powdered surgical screwdriver).

    FDA Recall
    Terminated ·Pro-Dex Inc·Product code MOQ·December 23, 2015

    Universal Battery Charger II (UBC II)

    FDA Recall
    Terminated ·The Anspach Effort, Inc.·Product code MOQ·January 15, 2016

    POWER MODULE F/TRS

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code MOQ·November 15, 2016

    BATTERY DEVICE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS·Product code MOQ·October 11, 2016