4 results
·
13ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Malfunction
×
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code FDF·July 24, 2021
POSTERIOR VITRECTOMY PACK
FDA Adverse Event
Malfunction
·BAUSCH & LOMB·Product code HQC·May 30, 2014
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)
FDA Adverse Event
Malfunction
·ALLERGAN·Product code LTI·December 20, 2010
CEMENT, BONE, VERTEBROPLASTY
FDA Adverse Event
Malfunction
·MEDTRONIC SOFAMOR DANEK·Product code NDN·February 15, 2013