13 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
IMPLANTABLE COLLAMER LENS (ICL)
FDA Adverse Event
Injury
·STAAR SURGICAL COMPANY·Product code MTA·April 5, 2018
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·March 27, 2013
TOTAL ASR ACET IMP SIZE 50
FDA Adverse Event
Injury
·DEPUY INTL., LTD. - 8010379·Product code KWA·March 2, 2011
THERMOPAD
FDA Adverse Event
Injury
·ANGIODYNAMICS, INC.·Product code GEI·April 2, 2008
MERSILENE TAPE UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code GAT·November 20, 2025
VALIANT CAPTIVIA UNK
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·July 13, 2023
VALIANT CAPTIVIA UNK
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·July 13, 2023
VALIANT CAPTIVIA UNK
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·July 13, 2023
HOSP SS FLEXX METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 12, 2011
HOSP SS FLEXX METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 12, 2011
HOSP SS FLEXX METER LASER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·June 17, 2011
HOSP SS FLEXX METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 12, 2011
UNSPECIFIED BD SECONDARY EXTENSION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FPA·September 24, 2022