10 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·March 25, 2013
ACRYSOF
FDA Adverse Event
Other
·ALCON RESEARCH. LTD./HUNTINGTON·Product code HQL·March 10, 2011
PRECISION XTRA/OPTIUM
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·March 26, 2008
PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT
FDA Adverse Event
Injury
·ETHICON INC.·Product code FTL·August 7, 2023
NV GXL LINER NEUTRAL, 32MM ID GROUP 1 CUPS
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JDI·September 2, 2022
FIRST MEDICAL SOURCE
FDA Adverse Event
Other
·B. BRAUN MEDICAL PRODUCTION LTD. EASTERN SEABOARD INDUS ESTATE·Product code MEB·September 26, 2011
FIRST MEDICAL SOURCE
FDA Adverse Event
Other
·MEDPRO INTERNATIONAL (THAILAND) LTD·Product code MEB·August 8, 2011
WOLF-PAK
FDA Adverse Event
Other
·B. BRAUN MEDICAL PRODUCTION LTD. E. SEABOARD INDUS ESTATE·Product code MEB·September 26, 2011
VIPAT
FDA Adverse Event
Other
·B. BRAUN MEDICAL PRODUCTION LTD.·Product code MEB·September 26, 2011
MEDPRO ACCUFLO WITH CHEMO INDICATION
FDA Adverse Event
Other
·B BRAUN MEDICAL PRODUCTION LTD·Product code MEB·September 26, 2011