20 results · 41ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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