25 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
Injury
·CONMED CORPORATION·Product code DRX·October 24, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·October 25, 2013
SYRINGE 1.0ML 30GA 8MM BLS 500CAS AP
FDA Adverse Event
Malfunction
·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·February 3, 2025
GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 29, 2021
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 8, 2014
8800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012
LANX SPINAL FIXATION SYSTEM
FDA Adverse Event
Malfunction
·LANX, INC.·Product code NKB·August 11, 2010
GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·August 4, 2021
SMR CEMENTL. REV. STEM Ø15 MM
FDA Adverse Event
Injury
·LIMACORPORATE SPA·Product code KWS·November 17, 2021
GORE® EXCLUDER® CONFORMABLE AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·December 22, 2023
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·November 19, 2013
SURETRACE ADULT ECG ELECTRODE
FDA Adverse Event
CONMED CORPORATION·Product code DRX·December 17, 2013
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 29, 2024