11 results
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44ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
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A&E MEDICAL MYOWIRE IIA&E MEDICAL MYOWIRE II
FDA Adverse Event
Malfunction
·ALTO DEVELOPMENT CORP·Product code GAO·July 22, 2015
PACING WIRE
FDA Adverse Event
Malfunction
·ALTO DEVELOPMENT CORP.·Product code LDF·April 4, 2000
A&E MEDICAL ELECTROSURGICAL PENCIL
FDA Adverse Event
Malfunction
·ALTO DEVELOPMENT CORP.·Product code GEI·October 30, 2008
WIRE TWSITER
FDA Adverse Event
Malfunction
·ALTO DEVELOPMENT CORP.·Product code HXS·November 15, 2016
MYO/PUNCH ROTATING SURGICAL PUNCH
FDA Adverse Event
Malfunction
·ALTO DEVELOPMENT CORP·Product code LRY·November 1, 2013
STERNAL NEEDLE DOUBLE WIRE BALL.CS#3.USP#6.65MM
FDA Adverse Event
Malfunction
·AE MEDICAL / ALTO DEVELOPMENT CORP.·Product code GAO·April 22, 2022
STERNALOCK XP RIGID FIXATION SYSTEM
FDA Adverse Event
Malfunction
·ZIMMER BIOMET/ALTO DEVELOPMENT CORP.·Product code HRS·June 17, 2024
ZIMMER BIOMET STERNALOCK XP RIGID FIXATION SYSTEM
FDA Adverse Event
Malfunction
·ALTO DEVELOPMENT CORP./A&E MEDICAL CORP.·Product code IKD·September 22, 2025
STERNALOCK X RIGID FIXATION SYSTEM IMPLANT X CABLE PLATE
FDA Adverse Event
Malfunction
·A&E MEDICAL CORP./ALTO DEVELOPMENT CORP.·Product code HRS·May 16, 2025
MYO/WIRE II
FDA Adverse Event
Malfunction
·ALTO DEVELOPMENT CORP, DBA A&E MEDICAL·Product code GAO·January 28, 2013
DISPOSABLE SUCTION COAGULATOR
FDA Adverse Event
Malfunction
·A&E MEDICAL CORPORATION / ALTO DEVELOPMENT CORP.·Product code GEI·July 25, 2023