18 results · 40ms · 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.

WALLSTENT RP ENDOPROSTHESIS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·April 19, 2023

WALLSTENT ENDOPROSTHESIS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 22, 2025

WALLSTENT ENDOPROSTHESIS

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code MAF·December 1, 2025

INTACS PRESCRIPTION INSERTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023

MAESTRO FOOT SWITCH

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·September 29, 2025

INTACS PRESCRIPTION INSERTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·November 3, 2023

INTACS CORNEAL IMPLANTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006

INTACS PRESCRIPTION INSERTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·April 3, 2006

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023

MAESTRO 4000 POD, 100W

FDA Adverse Event
Malfunction ·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023

MAESTRO 4000 CONTROLLER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 22, 2013

EEA 31

FDA Adverse Event
Malfunction ·COVIDIEN/TYCO·Product code GDW·February 1, 2011

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2014

INTACS PRESCRIPTION INSERTS

FDA Adverse Event
Injury ·ADDITION TECHNOLOGY, INC.·Product code LQE·June 20, 2006