9 results
·
31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TIBIAL INSERT FIXED SPHERE FLEX SIZE 2/13 MM R
FDA Adverse Event
Malfunction
·MEDACTA INTERNATIONAL SA·Product code JWH·June 15, 2018
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code NKB·May 1, 2014
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·July 6, 2025
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 2, 2012
CORAIL AMT COLLAR SIZE 11
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWA·October 15, 2014
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·July 22, 2011
BARD-PARKER SURGICAL BLADE
FDA Adverse Event
Other
·ASPEN SURGICAL PRODUCTS, INC.·Product code GES·May 31, 2013
ALPHA INSERT, PE, JJ/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWB·May 14, 2019
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code NKB·May 25, 2016