4,078 results · 28ms · 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.

PROMUS ELEMENT

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code NIQ·June 20, 2019

N/A

FDA Adverse Event
Malfunction ·ASCENT HEALTHCARE SOLUTIONS·Product code NLI·October 5, 2009

NOT KNOWN

FDA Adverse Event
Malfunction ·MEDTRONIC ENT·Product code NLY·January 19, 2007

N/A

FDA Adverse Event
Malfunction ·ASCENT·Product code NLI·January 7, 2011

N/A

FDA Adverse Event
Malfunction ·STRYKER SUSTAINABILITY SOLUTIONS·Product code NLI·November 1, 2011

N/A

FDA Adverse Event
Malfunction ·STRYKER SUSTAINABILITY SOLUTIONS·Product code NLI·December 16, 2011

N/A

FDA Adverse Event
Malfunction ·STRYKER SUSTAINABILITY SOLUTIONS·Product code NLI·August 17, 2012

OXIMAX DOC-10

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DPZ·January 11, 2013

ARROW CVC SET: 3-LUMEN 7 FR X 20 CM

FDA Adverse Event
Malfunction ·ARROW INTERNATIONAL INC.·Product code DQY·March 5, 2019

PLATE, FIXATION, BONE

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code HRS·April 17, 2015

FOCUS

FDA Adverse Event
Malfunction ·COMPUTERIZED MEDICAL SYSTEMS·Product code MUJ·September 18, 2001

HIGH FREQUENCY OSCILLATING VENTILATOR (HFOV)

FDA Adverse Event
Malfunction ·CAREFUSION·Product code LSZ·February 8, 2016

STERI-GAS, STERI-VAC

FDA Adverse Event
Malfunction ·3M·Product code FLI·January 18, 2002

STERI-GAS 4-100 CARTRIDGE

FDA Adverse Event
Malfunction ·3M·Product code FLI·September 19, 2000

STERI-GAS 4-100

FDA Adverse Event
Malfunction ·3M CO.·Product code FLI·September 12, 2000

STERI-GAS 4-100 CARTRIDGE

FDA Adverse Event
Malfunction ·3M CO.·Product code FLI·May 19, 2000

STERI-GAS 4-100 CARTRIDGE

FDA Adverse Event
Malfunction ·3M CO.·Product code FLI·January 21, 2000

PUMP MMT-1781KL 670G MG RPL

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·November 3, 2022

ELI

FDA Adverse Event
Malfunction ·MORTARA INSTRUMENT, INC.·Product code DPS·April 16, 2025

ELI 280

FDA Adverse Event
Malfunction ·MORTARA INSTRUMENT, INC.·Product code LOS·October 11, 2017