7 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LEVEL 1 HOTLINE DISPOSABLE ADMINISTRATION SETS
FDA Adverse Event
Malfunction
·SMITHS MEDICAL ASD; INC.·Product code LGZ·April 14, 2020
SPINALPAK(R) STIMULATOR ELECTRODES
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·March 14, 2017
SPINALPAK(R) STIMULATOR ELECTRODES
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·March 14, 2017
SPINALPAK(R) STIMULATOR ELECTRODES
FDA Adverse Event
Injury
·EBI, LLC.·Product code LOF·March 14, 2017
TOTAL ASR ACET IMP SIZE 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·June 4, 2014
HIRES 90K IMPLANT
FDA Adverse Event
Injury
·ADVANCED BIONICS, LLC·Product code MCM·November 26, 2012
SM204 M-SERIES W/BIG WHEEL
FDA Adverse Event
Malfunction
·STRYKER CORP. MEDICAL DIVISION·Product code FPO·September 27, 2010