13 results
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34ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
RULTRACT SKYHOOK RETRACTOR SYSTEM
FDA Adverse Event
Other
·PEMCO, INC.·Product code GAD·January 5, 2009
RULTRACT SEYHOOK RETRACTOR
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·July 22, 2003
RULTRACT SKYHOOK RETRACTOR
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·July 30, 2003
RULTRACT SKYHOOK RETRACTOR
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·July 22, 2003
RULTRACT
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·May 3, 2004
RULTRACT SKYHOOK RETRACTOR
FDA Adverse Event
Injury
·PEMCO, INC.·Product code GAD·April 29, 2011
RULTRACT SKYHOOK SURGICAL RETRACTOR SYSTEMS
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·March 26, 2015
RULTRACT SKYHOOK RETRACTOR SYSTEM
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·July 5, 2006
RULTRACT SKYHOOK RETRACTOR
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·December 20, 2013
RULTRACT SKYHOOK SURGICAL RETRACTOR SYSTEMS
FDA Adverse Event
PEMCO, INC.·Product code GAD·October 26, 2015
RULTRACT SKYHOOK
FDA Adverse Event
Malfunction
·PEMCO, INC.·Product code GAD·December 21, 2002
PEMCO MEDICAL PERFUSION PUMP
FDA Adverse Event
Death
·PEMCO MEDICAL, INC.·Product code KFM·April 7, 2005
UNK
FDA Adverse Event
Injury
·GRAHAM-FIELD TEMCO, INC·Product code FRJ·March 18, 1999