9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DRILL, AO, STERILE 4, 2X340 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·September 23, 2011
1.5MM CANN. QUICK RELEASE DRIVER TIP
FDA Adverse Event
Malfunction
·ACUMED, LLC·Product code LXH·June 14, 2024
1.5MM CANN. QUICK RELEASE DRIVER TIP
FDA Adverse Event
Malfunction
·ACUMED, LLC·Product code LXH·June 14, 2024
SCREW, FIXATION, BONE
FDA Adverse Event
Malfunction
·ACUMED, LLC·Product code HWC·June 14, 2024
INSPIRA TEXTURED SILICONE GEL FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FTR·May 28, 2025
UNIV-BATTERY CHARGER F/SYNTHES BATT 4 CH
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code MOQ·November 14, 2014
EON MINI IPG, 16-CHANNEL RECHARGEABLE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·September 12, 2011
2520274-2013-04657
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·July 29, 2013
TAPERLOC 133 FP TYPE1 PPS HO 5.0 T1
FDA Adverse Event
Malfunction
·ZIMMER BIOMET, INC.·Product code KWA·March 30, 2020