997 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·March 8, 2023
PACS SERVER
FDA Adverse Event
Malfunction
·GE HEALTHCARE·Product code LLZ·June 26, 2009
ENDO GIA
FDA Adverse Event
Injury
·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·August 16, 2018
CARDIOSAVE HYBRID, TYPE G PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP. - MAHWAH·Product code DSP·February 24, 2023
BD VACUTAINER® SAFETY-LOK¿ BLOOD COLLECTION SET
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code JKA·August 31, 2022
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·September 9, 2025
CARDIOSAVE HYBRID, TYPE G PLUG
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·March 19, 2024
UNKNOWN LIGASURE INSTRUMENT
FDA Adverse Event
Injury
·COVIDIEN MFG DC BOULDER·Product code GEI·May 20, 2024
PERFUSOR®
FDA Adverse Event
Malfunction
·B BRAUN MELSUNGEN AG·Product code FRN·September 25, 2023
BD BBL¿ MGIT¿ MYCOBACTERIA GROWTH INDICATOR TUBES, 7ML
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code MDB·May 7, 2022
UNKNOWN ENDO GIA SULU
FDA Adverse Event
Injury
·COVIDIEN SURGICAL·Product code GDW·April 16, 2026
CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·January 20, 2025
LIVER ACCESS AND BIOPSY SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FCG·March 3, 2026
BARDEX® LUBRI-SIL® ALL-SILICONE FOLEY CATHETER
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·February 5, 2025
INFUSOMAT SPACE
FDA Adverse Event
Malfunction
·B.BRAUN MELSUNGEN AG·Product code FRN·March 30, 2022
INFUSOMAT SPACE
FDA Adverse Event
Malfunction
·B.BRAUN MELSUNGEN AG·Product code FRN·March 30, 2022
ARCHITECT HBSAG QUALITATIVE II CONFIRMATORY
FDA Adverse Event
Malfunction
·ABBOTT IRELAND·Product code KSJ·October 21, 2019
INFUSOMAT SPACE
FDA Adverse Event
Malfunction
·B.BRAUN MELSUNGEN AG·Product code FRN·August 9, 2022
TENS UNIT
FDA Adverse Event
Malfunction
·PAIN MANAGEMENT TECHNOLOGIES·Product code NUH·October 4, 2016
OMRON ELECTROTHERAPY PAIN RELEIF
FDA Adverse Event
Injury
·OMRON (DALIAN) CO., LTD. (PLANT 2)·Product code NUH·September 21, 2015