498 results
·
53ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
SENSICLIP
FDA Adverse Event
Malfunction
·CAREFUSION 213 LLC·Product code LWK·November 25, 2016
N/A
FDA Adverse Event
CAREFUSION 213 LLC·Product code LWK·January 28, 2014
*
FDA Adverse Event
CAREFUSION 213 LLC·Product code LWK·January 16, 2014
N/A
FDA Adverse Event
CAREFUSION 213 LLC·Product code LWK·January 28, 2014
N/A
FDA Adverse Event
Malfunction
·CAREFUSION 213 LLC·Product code LWK·February 5, 2014
*
FDA Adverse Event
Malfunction
·CAREFUSION 213 LLC·Product code LWK·May 29, 2013
CHLORAPREP ONE STEP
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC·Product code KXG·April 18, 2024
RAZOR, SURGICAL
FDA Adverse Event
Malfunction
·CAREFUSION 213 LLC·Product code LWK·December 1, 2016
CAREFUSION SURGICAL CLIPPER
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC·Product code LWK·October 24, 2016
*
FDA Adverse Event
Malfunction
·CAREFUSION 213 LLC·Product code LWK·November 19, 2013
CHLORAPREP UNKNOWN
FDA Adverse Event
Injury
·CAREFUSION 213, LLC 0113·Product code KXG·May 24, 2021
CHLORAPREP ONE STEP HI-LITE ORANGE
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·May 13, 2021
CHLORAPREP ONE STEP HI-LITE ORANGE
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·May 31, 2021
CHLORAPREP UNKNOWN
FDA Adverse Event
Injury
·CAREFUSION 213, LLC 0113·Product code KXG·April 15, 2021
CHLORAPREP ONE STEP HI-LITE ORANGE
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·June 21, 2021
CHLORAPREP UNKNOWN
FDA Adverse Event
Injury
·CAREFUSION 213, LLC 0113·Product code KXG·April 7, 2021
CHLORAPREP ONE STEP HI-LITE ORANGE
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·April 12, 2021
UNKNOWN CHLORAPREP
FDA Adverse Event
Injury
·CAREFUSION 213, LLC 0113·Product code KXF·June 15, 2021
CHLORAPREP ONE STEP HI-LITE ORANGE
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·May 25, 2021
CHLORAPREP ONE STEP HI LITE ORANGE
FDA Adverse Event
Malfunction
·CAREFUSION 213, LLC 0113·Product code KXG·May 4, 2021