9 results
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39ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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SENTRANT INTRODUCER SHEATH
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code DYB·May 21, 2020
1000 ML TPN BAG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·December 9, 2020
VENTED MICRO VOL.INLET, N/S
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·March 28, 2022
250 ML TPN BAG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code LHI·May 21, 2021
BELLATEK® ZIRCONIA ABUTMENT
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·June 27, 2014
MAXCEM ELITE
FDA Adverse Event
Injury
·KERR CORPORATION·Product code EMA·January 7, 2013
HX2 TEMPERATURE MANAGEMENT SYSTEM
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·October 29, 2010
ACCUTRAK DELIVERY CATHETER SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 9, 2020
ENVEO R DELIVERY SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·June 9, 2020