598 results
·
35ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
TIDI PRODUCTS ZERO-GRAVITY
FDA Adverse Event
Malfunction
·TIDI PRODUCTS, LLC·Product code EAJ·December 8, 2016
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·Product code KMK·October 1, 2021
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·TIDI PRODUCTS LLC·Product code KMK·December 30, 2021
TIDI PRODUCTS LLC, PEN BLADE
FDA Adverse Event
Malfunction
·TIDI PRODUCTS, LLC·Product code GDX·December 17, 2021
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·Product code KMK·October 9, 2021
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·Product code KMK·September 30, 2021
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·Product code KMK·September 29, 2021
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·TIDI PRODUCTS, LLC·Product code KMK·February 17, 2022
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·TIDI PRODUCTS, LLC·Product code KMK·February 11, 2022
TIDI PRODUCTS, LLC GRIP-LOK
FDA Adverse Event
Malfunction
·TIDI PRODUCTS, LLC·Product code KMK·January 26, 2022
SINGLE PATIENT GAIT BELT LONG
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code IKX·May 20, 2022
SINGLE PATIENT GAIT BELT LONG
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code IKX·June 7, 2022
SINGLE PATIENT USE GAIT BELT
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code IKX·June 21, 2022
SINGLE PATIENT GAIT BELT LONG
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code IKX·May 20, 2022
ALARM SENSOR, EZ CLEAN ALARM BELT
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code PJP·June 2, 2022
LOCKING TWICE-AS-TOUGH CUFFS
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code FMQ·April 20, 2022
SITTER ON CUE
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code PJO·June 6, 2022
SINGLE PATIENT GAIT BELT LONG
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code IKX·April 6, 2022
SINGLE PATIENT GAIT BELT LONG
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code IKX·June 22, 2022
SINGLE PATIENT USE GAIT BELT
FDA Adverse Event
Malfunction
·TIDI PRODUCTS·Product code IKX·April 14, 2022