13 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 29, 2025
PRECISION SPECTRA
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·August 16, 2019
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·May 1, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011
SOLETRA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·August 7, 2008
3.0MM TI W/ MAXBRAID SUTURE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWC·October 4, 2012
3.0MM TI W/ MAXBRAID SUTURE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWC·October 4, 2012
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code MMY·March 17, 2014
3.0MM TI W/ MAXBRAID SUTURE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code HWC·October 4, 2012
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORPORATION·Product code DXE·October 23, 2012
THROMBUSTER II
FDA Adverse Event
Malfunction
·KANEKA CORP.·Product code DXE·December 21, 2012
THROMBUSTER II
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code DXE·January 16, 2019
EUFLEXXA
FDA Adverse Event
Injury
·BIO-TECHNOLOGY GENERAL (ISRAEL) LTD.·Product code MOZ·February 23, 2015