8 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PINN MAR 10D +4 26IDX44OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·December 3, 2010
12/14 ARTICUL 40MM M SPEC+5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·January 17, 2013
VIVA QUAD XT
FDA Adverse Event
Death
·IPG MFG SWITZERLAND·Product code NIK·July 8, 2014
TSS KEELED GLENOID S
FDA Adverse Event
Malfunction
·ASCENSION ORTHOPEDICS·Product code KWS·March 24, 2015
REAGENT RED BLOOD CELLS IH-CELL A1 & B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·November 20, 2019
REAGENT RED BLOOD CELLS IH-CELL A1 & B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·November 20, 2019
REAGENT RED BLOOD CELLS IH-CELL A1 & B
FDA Adverse Event
Malfunction
·BIO-RAD MEDICAL DIAGNOSTICS GMBH·Product code QHT·November 20, 2019
BLOOD PUMP PU VALVES 10 ML, IN/OUT 6 MM
FDA Adverse Event
Malfunction
·BERLIN HEART GMBH·Product code DSQ·October 8, 2020