9 results
·
17ms
·
Sources: EU EUDAMED, US FDA
SAS SHIGELLA BOYDII TYPE 12 ANTISERUM
FDA 510(k)
FDA Class 2
·Microbiology
DOLOMITE MAXI ROLLATOR 650 7331492560417
FDA Adverse Event
Malfunction
·DOLOMITE AB·Product code ITJ·January 15, 2015
PROCERA ZIRCONIA ABUTMENT FOR CAMLOG IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
BUNNY ELECTRODE/STEALTH ELECTRODE PRE WIRED EEG
FDA 510(k)
FDA Class 2
·Cardiovascular
IMPELLA CP
FDA Adverse Event
Death
·ABIOMED, INC.·Product code OZD·January 4, 2026
ENTERALITE INFINITY ENTERAL FEEDING PUMP
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICES GROUP·Product code LZH·January 17, 2013
COULTER® ACT DIFF 2 ANALYZER
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GKZ·January 14, 2011
ANTHEM RF
FDA Adverse Event
Death
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 28, 2014
4.0MM TI LOCKING SCREW W/T25 STARDRIVE 40MM FOR IM NAILS
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HSB·December 22, 2020