7 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
I-PORT ADVANCE
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·October 3, 2025
DA VINCI ROBOTICS SYSTEM
FDA Adverse Event
Injury
·INTUITIVE SURGICAL, INC.·Product code NAY·October 21, 2003
MA204
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·March 13, 2013
UNKNOWN DEPUY ASR HIP
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·February 16, 2011
BARD COMPOSIX KUGEL HERNIA PATCH
FDA Adverse Event
Injury
·BARD·Product code FTL·February 21, 2008
TECNIS IOL
FDA Adverse Event
Malfunction
·AMO PUERTO RICO MFG. INC.·Product code MFK·November 4, 2024
HEARTWARE VENTRICULAR ASSIST SYSTEM - SHOULDER PACK
FDA Adverse Event
Malfunction
·HEARTWARE, INC.·Product code DSQ·August 1, 2023