7 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BEARING 28 MM I.D. 44 MM O.D. SIZE F
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·March 4, 2025
LINOX S 65
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NVY·October 2, 2013
DUAL TRIGGER WIRE COLLET
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·January 29, 2019
PRECISION®
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 27, 2014
7700
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 26, 2013
MUSTANG BALLOON DILATATION CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code LIT·August 11, 2011
G7 DUAL MOBILITY ACETABULAR SYSTEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·March 4, 2025