20 results
·
32ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
TORQ STERNAL CLOSURE DEVICE
FDA Adverse Event
Malfunction
·KARDIUM INC.·Product code LXH·September 10, 2012
SAFETY SCALPEL WITH POLYMER COATED SURGICAL BLADE
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC·Product code GDX·September 22, 2015
SOUTHMEDIC NON-STERILE DISPOSABLE SAFETY SCALPEL
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code GES·May 11, 2021
SOUTHMEDIC NON-STERILE DISPOSABLE SAFETY SCALPEL
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code GES·May 11, 2021
SOUTHMEDIC #10R DISPOSABLE SCALPEL NON-STERILE
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code GES·May 20, 2022
PERSONNA
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC.·Product code GES·December 3, 2009
SOUTHMEDIC SPSS CARTRIDGE
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC.·Product code GES·November 15, 2010
OXYMASK O2 KID
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code BYG·May 16, 2019
OXYMASK
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code BYG·September 14, 2022
SOUTHMEDIC SCALPEL
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code GES·November 30, 2023
SOUTHMEDIC POLYMER COATED SURGICAL BLADE
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC.·Product code GES·December 23, 2011
PERSONA
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC·Product code GES·November 23, 2011
SOUTHMEDIC #10R DISPOSABLE SCALPEL NON-STERILE
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code GES·November 17, 2022
OXYMASK ADULT ETCO2
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC.·Product code CCK·July 5, 2018
OXY2MASK O2/ETCO2 ADULT
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC·Product code CCK·April 22, 2025
SOUTHMEDIC SCALPEL
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC.·Product code GES·November 30, 2023
SOUTHMEDIC #10R DISPOSABLE SCALPEL NON-STERILE
FDA Adverse Event
Malfunction
·SOUTHMEDIC INC.·Product code GES·November 23, 2022
SOUTHMEDIC SAFETY SCALPEL
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC.·Product code GES·October 16, 2015
*
FDA Adverse Event
Malfunction
·SOUTHMEDIC, INC.·Product code GES·June 25, 2015
COULTER® LH 500 HEMATOLOGY ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·April 20, 2012