3 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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EM ESPE SCOTCHBOND UNIVERSAL
FDA Adverse Event
3M DEUTSCHLAND GMBH·Product code KLE·May 15, 2014
R SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION, WORLD WIDE HEADQUARTERS·Product code MKJ·October 19, 2012
LAP-BAND AP ADJUSTABLE GASTRIC BANDING SYSTEM (LARGE)
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·September 13, 2010