26 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 9, 2025
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
LOCKING CAP
FDA Adverse Event
Injury
·SYNTHES (USA)·Product code KTT·October 19, 2012
EON MINI
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 10, 2013
LAMITRODE S8
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·September 17, 2014
MINI TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LOX·June 3, 2011
COMP RVRS SHLDR GLNSP +6 36MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·March 24, 2021
SM HYBRID GLENOID BASE 4MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·September 1, 2021
PC HYBRID GLEN POST- POLY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·September 1, 2021
COMPREHENSIVE PT HYBRID GLEN POST REGENEREX
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·November 11, 2019
U BY KOTEX SLEEK
FDA Adverse Event
Malfunction
·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·August 31, 2018
COMPREHENSIVE VERSA-DIAL 46X24X47 HUMERAL HEAD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·September 6, 2018
HYBRID GLENOID BASE 4 MM SMALL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWS·August 11, 2017
COMPREHENSIVE SHOULDER SYSTEM MINI HUMERAL STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·August 11, 2017
MINI TRAY STD COCR +0 OFFSET
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·March 24, 2021
COMPREHENSIVE SHOULDER SYSTEM STANDARD TAPER ADAPTOR
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code MBF·August 11, 2017
U BY KOTEX SLEEK
FDA Adverse Event
Malfunction
·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·June 27, 2018
VERSA-DIAL/COMP TI STD TAPER
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code MBF·November 15, 2022