BEUDAMED
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    Filters FDA Adverse Event ×

    ALARIS PUMP MODULE ADMINISTRATION SET

    FDA Adverse Event
    Malfunction ·CAREFUSION CORP.·Product code FPA·January 15, 2014

    UNKNOWN RIGHT REJUVENATE/AGBII HIP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·October 24, 2012

    PORTEX TRACHEOSTOMY TUBE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL INTERNATIONAL LTD·Product code BTO·June 1, 2015

    ARCOM XL 44-36 RTNV+3 HMRL BRG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·October 10, 2017

    COMP RVRS SHLDR GLNSP STD 36MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PAO·October 12, 2017