7 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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CHECK-IT
FDA Adverse Event
Malfunction
·LUCIRA HEALTH, INC.·Product code QJR·May 15, 2022
SPINAL NEEDLE 27GA 3.50 IN
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code MIA·November 28, 2023
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014
HEARTSTREAM FR2
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 26, 2013
SYNCHROMED II
FDA Adverse Event
Malfunction
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·August 3, 2011
A200 KNEE SYSTEM
FDA Adverse Event
Injury
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016
A200 KNEE SYSTEM
FDA Adverse Event
Injury
·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016