14 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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IPL HAIR REMOVAL DEVICE CT05
FDA Adverse Event
Injury
·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·February 19, 2026
HAND-HELD HAIR REMOVAL DEVICE
FDA Adverse Event
Injury
·SHENZHEN CHUANGTONG YIGOU TECHNOLOGY CO., LTD.·Product code OHT·March 9, 2026
CD1800 ANALYZER
FDA Adverse Event
Other
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·November 30, 2007
EON MINI
FDA Adverse Event
Injury
·ST. JUDE MED - NEUROMODULATION·Product code GZB·November 12, 2014
ACCU-CHEK FLEXLINK PLUS
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC.·Product code LZG·August 31, 2011
GALAXY INTRAVASCULAR ULTRASOUND SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - FREMONT (SUD)·Product code IYO·July 29, 2013
APEX KNEE SYSTEM
FDA Adverse Event
Injury
·OMNILIFE SCIENCE INC.·Product code JWH·March 3, 2023
APEX KNEE SYSTEM
FDA Adverse Event
Injury
·OMNILIFE SCIENCE INC.·Product code JWH·April 11, 2023
APEX KNEE SYSTEM
FDA Adverse Event
Injury
·OMNILIFE SCIENCE INC.·Product code JWH·June 20, 2023
AIA-900
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·October 20, 2017
ATELLICA IM 1300 ANALYZER
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·May 5, 2022
AIA-360
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·October 20, 2017
AIA-2000
FDA Adverse Event
Malfunction
·TOSOH CORPORATION·Product code KHO·October 20, 2017
AIA-360
FDA Adverse Event
Malfunction
·TOSOH HI-TEC·Product code KHO·September 6, 2017