8 results
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39ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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BINAXNOW¿ COVID-19 AG CARD
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·January 4, 2022
BINAXNOW¿ COVID-19 AG CARD
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·January 4, 2022
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 10, 2011
ACCU-CHEK ® COMPACT PLUS TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·October 24, 2014
GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·July 1, 2013
PROTECTION PLUS IV CATHETER 226 1" #2000-06
FDA Adverse Event
Injury
·JOHNSON & JOHNSON MEDICAL INC.·Product code FOZ·September 18, 1997
REGENT HEART VALVE
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code LWQ·October 21, 2022
PADPRO:AD;RTRANS EL/LW, 12X7
FDA Adverse Event
Injury
·KATECHO, INC.·Product code MKJ·October 7, 2022