597 results
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30ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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O-ARM O2 IMAGING SYSTEM
FDA Adverse Event
Malfunction
·SANMINA -SCI SYSTEMS·Product code OWB·March 13, 2025
NEURO SPG-1X1"-STERILE- 20/CS
FDA Adverse Event
Malfunction
·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 20, 2025
NEURO SPNG-1/2X3"-STRL- 20/CS
FDA Adverse Event
Malfunction
·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025
NEURO-SP-1/2X1/2"-STRL 20/CS
FDA Adverse Event
Malfunction
·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025
NEURO-SP-1/2X1/2"-STRL 20/CS
FDA Adverse Event
Malfunction
·MEDSORB DOMINICANA, S.A.·Product code EFQ·January 20, 2025
NEURO-SP-1/2X1/2"-STRL 20/CS
FDA Adverse Event
Malfunction
·MEDSORB DOMINICANA, S.A.·Product code EFQ·February 7, 2025
VISTEC SPG 4X4 NON ST 10S 16PLY
FDA Adverse Event
Malfunction
·COVIDIEN·Product code EFQ·November 1, 2016
VISTEC SPG 4X8 NON ST 10S 16PLY
FDA Adverse Event
Malfunction
·AUGUSTA·Product code EFQ·November 1, 2016
VISTEC SPG 4X4 STR 10S 16 PLY
FDA Adverse Event
Malfunction
·COVIDIEN·Product code EFQ·December 8, 2016
KITTNER (BLUNT) DISSECTOR
FDA Adverse Event
Malfunction
·MEIXIN MEDICAL SUZHOU CO., LTD.·Product code EFQ·October 31, 2016
EXCILON
FDA Adverse Event
Malfunction
·COVIDIEN·Product code EFQ·March 16, 2012
PACK VAGINAL PREP SCRB + PNT
FDA Adverse Event
Malfunction
·COVIDIEN·Product code EFQ·January 24, 2012
DEROYAL
FDA Adverse Event
Malfunction
·CARWILD CORP·Product code EFQ·June 17, 2014
DEROYAL
FDA Adverse Event
Malfunction
·CARWILD CORP·Product code EFQ·June 17, 2014
*
FDA Adverse Event
SRI/SURGICAL EXPRESS, INC.·Product code EFQ·February 10, 2010
PILLING NEURO SPONGE 1X2" X 1/2"
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code EFQ·June 30, 2010
DEROYAL
FDA Adverse Event
Malfunction
·CARWILD CORP.·Product code EFQ·June 20, 2014
NEURO SPONGE PATTIES
FDA Adverse Event
Malfunction
·DEROYAL INDUSTRIES, INC.·Product code EFQ·April 21, 2022
BARCODE PACK
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code EFQ·April 19, 2012
KERLIX DISP LAP SPONGE
FDA Adverse Event
Malfunction
·AUGUSTA·Product code EFQ·February 20, 2002