20 results
·
41ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
NAVIX ACCESS DEVICE
FDA Adverse Event
Injury
·XLUMENA, INC.·Product code GCJ·October 15, 2010
NAVIX ACCESS DEVICE
FDA Adverse Event
Injury
·XLUMENA INC.·Product code GCJ·August 22, 2011
NAVIX ACCESS DEVICE
FDA Adverse Event
Injury
·XLUMENA, INC.·Product code GCJ·April 4, 2011
AXIOS STENT AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·XLUMENA INC.·Product code PCU·March 27, 2015
AXIOS STENT AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·XLUMENA INC., A BOSTON SCIENTIFIC COMPANY·Product code PCU·June 16, 2015
AXIOS STENT AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·XLUMENA INC., BOSTON SCIENTIFIC CO·Product code PCU·June 11, 2015
BIOGLUE- UNKNOWN CONFIGURATION
FDA Adverse Event
Injury
·ARTIVION, INC.·Product code MUQ·April 26, 2024
IMPELLA
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code OZD·March 30, 2026
IMPELLA
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code OZD·May 14, 2026
IMPELLA
FDA Adverse Event
Injury
·ABIOMED, INC. - 1220648·Product code OZD·April 17, 2026
TURBO-JECT® DOUBLE LUMEN POWER-INJECTABLE PICC
FDA Adverse Event
Injury
·COOK INC·Product code LJS·September 17, 2018
LEMAITRE SINGLE LUMEN EMBOLECTOMY CATHETER
FDA Adverse Event
Injury
·LEMAITRE VASCULAR, INC.·Product code DXE·February 12, 2016
BIOGLUE SURGICAL ADHESIVE
FDA Adverse Event
Injury
·CRYOLIFE, INC.·Product code MUQ·June 5, 2013
RELAY PRO THORACIC STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL INC.·Product code MIH·September 13, 2023
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·September 6, 2023
GORE® EXCLUDER® AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 7, 2022
TURBO-JECT® DOUBLE LUMEN POWER-INJECTABLE PICC
FDA Adverse Event
Injury
·COOK INC·Product code LJS·September 18, 2018
CONFORMABLE GORE® TAG®THORACIC ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·May 28, 2025
GORE® MOLDING & OCCLUSION BALLOON CATHETER
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 7, 2022
ASAHI CARAVEL
FDA Adverse Event
Injury
·ASAHI INTECC CO., LTD.·Product code DQY·June 25, 2018