9 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·September 17, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·September 17, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·September 17, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCABOROUGH·Product code QJR·September 17, 2021
BINAX NOW COVID-19 AG CARD
FDA Adverse Event
Injury
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 13, 2021
GREENLIGHT HPS BPH FIBER OPTIC
FDA Adverse Event
Malfunction
·AMS INNOVATIVE CENTER-SAN JOSE·Product code GEX·March 29, 2013
EXPO GUIDE CATHETER
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQO·March 29, 2011
INDURA
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code LKK·April 23, 2008
DEPTH GAUGE FOR 2.0MM AND 2.4MM SCREWS
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code HTJ·August 5, 2016