14 results · 23ms · Sources: EU EUDAMED, US FDA

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OT VERIO FLEX METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE GMBH·Product code NBW·May 21, 2019

WRIST BLOOD PRESSURE UNIT

FDA Adverse Event
Malfunction ·MEDLINE INDUSTRIES, LP - NORTHFIELD·Product code DXN·July 12, 2022

STEM: AMISTEM C CEMENTED STD SIZE 2

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·February 3, 2021

IMPAX CV REPORTING

FDA Adverse Event
Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·June 11, 2013

ESPRIT VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·July 15, 2011

TRIDENT HEMISPHERICAL CLUSTER 58MM

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·September 16, 2008

COOK® SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·May 17, 2019

COOK® SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·March 18, 2019

OPTILITE SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·June 5, 2020

COOK® SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·March 12, 2019

COOK® SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·March 18, 2019

COOK® SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Injury ·COOK INC·Product code GEX·November 4, 2022

OPTILITE SINGLE-USE HOLMIUM LASER FIBER

FDA Adverse Event
Malfunction ·COOK INC·Product code GEX·February 13, 2020

NIPRO BLOOD TUBING SET W/TRANSDUCER PROTECTOR

FDA Adverse Event
Injury ·NIPRO (THAILAND) CORP., LTD.·Product code FJK·March 16, 2018