20 results · 32ms · Sources: EU EUDAMED, US FDA

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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