13 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
CHLORAPREP ONE STEP
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·April 19, 2021
CHLORAPREP ONE STEP FREPP
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXF·May 26, 2021
CHLORAPREP ONE STEP
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·September 15, 2021
CHLORAPREP ONE-STEP
FDA Adverse Event
Malfunction
·CAREFUSION, INC·Product code KXG·November 24, 2020
CHLORAPREP ONE STEP FREPP
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·May 26, 2021
CHLORAPREP ONE STEP FREPP
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·August 24, 2021
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 25, 2013
UNKNOWN SPINAL CORD STIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LGW·November 24, 2010
GMK-REVISION TIBIAL AUGMENTATION SIZE 5/10MM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KRO·August 30, 2018
GMK HINGE FIXED TIBIAL INSERT # 1/10MM
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KRO·October 24, 2015
CHLORAPREP ONE STEP FREPP
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·August 18, 2021
ASTROGLIDE
FDA Adverse Event
Malfunction
·COMBE INC·Product code KMJ·January 16, 2024
GMK-HINGE FEMORAL COMPONENT SIZE 3 R
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code KRO·September 14, 2018