11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORP·Product code MKJ·February 4, 2014
M2A 38MM MODULAR HEAD STD NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·October 31, 2012
CONSTRAINED ACETABULAR INSERTS
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code KWZ·August 16, 2010
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 4, 2022
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 4, 2022
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 4, 2022
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 3, 2022
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 4, 2022
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 4, 2022
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 3, 2022
PORTEX TUBES BLUE LINE ULTRA (BLU)
FDA Adverse Event
Malfunction
·SMITHS MEDICAL INTERNATIONAL, LTD.·Product code BTO·November 4, 2022