9 results
·
32ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 17, 2025
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 2, 2025
POLIGRIP ORIGINAL AND SUPER POLIGRIP
FDA Adverse Event
Other
·GLAXOSMITHKLINE·Product code KOL·February 2, 2010
UNKNOWN_SPINE_PRODUCT
FDA Adverse Event
Malfunction
·STRYKER SPINE-FRANCE·Product code LXH·March 19, 2013
RIATA ACTIVE FIXATION LEAD
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·May 1, 2014
ENDOPATH ETS FLEX
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code KOG·September 11, 1997
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·April 28, 2014
COULTER ISOTON III DILUENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER·Product code GIF·March 27, 2014