13 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 29, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·November 5, 2020
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·April 14, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH,INC.·Product code QJR·April 14, 2021
PROCLAIM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 1, 2017
SOLETRA
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 14, 2012
ARCHITECT IPTH
FDA Adverse Event
Malfunction
·ABBOTT GERMANY·Product code CEW·March 13, 2013
ASR ACETABULAR CUPS 48
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 18, 2011
UNK DEPUY FEMORAL COMPONENT
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HSA·February 20, 2008
ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE TIBIAL BUSHING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018
ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE FEMORAL BUSHING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018
ORTHOPEDIC SALVAGE SYSTEM LOCKING PIN
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018
ORTHOPEDIC SALVAGE SYSTEM POLYETHYLENE BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JDI·January 11, 2018