11 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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UNKNOWN PLASMABLADE DEVICE
FDA Adverse Event
Malfunction
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·August 4, 2014
PULSAR 2 GENERATOR
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY·Product code MUL·August 4, 2014
PLASMABLADE 3.0 WIDE SPATULA
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·August 4, 2014
CUP: MPACT ACETABULAR SHELL Ø48 NO-HOLE
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LPH·January 4, 2023
LEADER 1CC X 31G INS SYR
FDA Adverse Event
Malfunction
·COVIDIEN·Product code FMF·February 25, 2013
SECUR-FIT HA PSL CUP/CLUSTER SHELL 50MM
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·March 1, 2011
CONTOUR TEST STRIPS (10)
FDA Adverse Event
Malfunction
·BAYER HEALTHCARE, LLC·Product code NBW·March 11, 2008
GENERATOR PULSAR II
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code MUL·August 22, 2014
A7 ANESTHESIA SYSTEM
FDA Adverse Event
Malfunction
·SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO. LTD.·Product code BSZ·February 15, 2017
PLASMABLADE 4.0 GENERAL SURGERY
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·August 22, 2014
PLASMABLADE 4.0 GENERAL SURGERY
FDA Adverse Event
Injury
·MEDTRONIC ADVANCED ENERGY, LLC·Product code DWG·August 22, 2014