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

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BECKMAN COULTER ¿ COULTER ® LH 750 HEMATOLOGY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER INC.·Product code GKZ·September 26, 2011

640G INSULIN PUMP MMT-1711K

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 12, 2022

640G INSULIN PUMP MMT-1711K

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 12, 2022

KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code DYB·February 19, 2026

CELSIUS¿ ELECTROPHYSIOLOGY CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC.·Product code LPB·August 9, 2019

SETSCREW

FDA Adverse Event
Malfunction ·Product code NKB·September 22, 2023

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 12, 2026

THERMOCOOL® SF UNI-DIRECTIONAL CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·November 21, 2018

PRLNE BLU 24IN 7-0 D/A BV-1

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAW·September 20, 2024

PRLNE BLU 30IN 6-0 D/A C-1

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAW·September 24, 2024

PRLNE BLU 30IN 6-0 D/A C-1

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAW·September 24, 2024

PRLNE BLU 24IN 7-0 D/A BV-1

FDA Adverse Event
Malfunction ·ETHICON INC.·Product code GAW·September 20, 2024

PTS TUBING PACK

FDA Adverse Event
Malfunction ·LIVANOVA USA INC.·Product code DWE·February 6, 2024

CARDIOPLEGIA PACKS, PERFUSION TUBING SET, PERFUSION TUBING, TUBING

FDA Adverse Event
Malfunction ·LIVANOVA INC. USA·Product code DWE·January 10, 2024

INPEN MMT-105NNBLNA NOVO NORDISK BLUE

FDA Adverse Event
Malfunction ·COMPANION MEDICAL INC·Product code FMF·June 1, 2021

PUMP 371 14F LT CMR SET

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 19, 2026

KIT, 23FR INTRODUCER, 11CM, STERILE

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 18, 2026

ESOPHYX Z+

FDA Adverse Event
Injury ·ENDOGASTRIC SOLUTIONS INC·Product code ODE·August 27, 2024

IMPELLA

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 12, 2026