8 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
APC PLUS ADHESIVE
FDA Adverse Event
Injury
·3M UNITEK·Product code DYW·June 7, 2007
UNKNOWN MAXIM BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·May 8, 2014
IMPLANT PDS3000M 6PK PILLAR PALATAL
FDA Adverse Event
Injury
·XOMED MFG JACKSON·Product code LRK·October 17, 2012
G2 X FILTER SYSTEM - JUGULAR
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·August 4, 2010
PUREWICK FEMALE EXTERNAL CATHETER
FDA Adverse Event
Injury
·C.R. BARD INC. (COVINGTON) -1018233·Product code NZU·September 17, 2025
UNKNOWN PUREWICK URINE COLLECTION SYSTEM
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code NZU·October 17, 2025
PUREWICK MALE EXTERNAL CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code NZU·February 19, 2026
PUREWICK URINE COLLECTION SYSTEM
FDA Adverse Event
Malfunction
·C.R. BARD INC. (COVINGTON) -1018233·Product code NZU·January 9, 2026