4 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
BD BACTEC¿ MGIT¿ 960 SUPPLEMENT KIT
FDA Adverse Event
Malfunction
·LEE LABORATORIES, INC.·Product code MDB·August 12, 2022
ALARIS SYSTEM PUMP MODULE
FDA Adverse Event
Injury
·CARDINAL HEALTH ALARIS PRODUCTS·Product code FRN·December 10, 2008
TOTAL ASR FEM IMP SIZE 55
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KXA·September 22, 2011
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 2, 2013