3 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CAPSUREEPI
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DTB·April 30, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 10, 2012
BATTERY F/NOS. 532.101+532.110
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code HWE·May 19, 2015