9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
LIFEPAK CR® PLUS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·October 23, 2012
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 30, 2013
ADULT NASAL INTERFACE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code CAT·August 17, 2010
SURE-T PARADIGM
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 30, 2024
ACTIVELIFE
FDA Adverse Event
Malfunction
·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·November 7, 2019
ACTIVELIFE
FDA Adverse Event
Malfunction
·CONVATEC DOMINICAN REPUBLIC INC·Product code EZQ·November 7, 2019
T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY
FDA Adverse Event
Malfunction
·TANDEM DIABETES CARE·Product code QFG·October 5, 2022
SURE-T PARADIGM
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·February 21, 2025
SURE-T PARADIGM
FDA Adverse Event
Malfunction
·UNOMEDICAL UM-D·Product code FPA·February 21, 2025