InjuryFAF
SALINE TESTICULAR, LARGE
Received Apr 28, 2005 · Event occurred Mar 21, 2005
Report 2125050-2005-00117 · MDR key 596671
Device
Generic name
Testicular Product
Manufacturer
Mentor Corporation - Minnesota DivisionModel number
450-1329Catalog number
450-1329
Lot number
953
Product problems
- Implant, removal of
Patient
42 YR
- Unspecified Infection
- Hospitalization required
Narrative
Description of Event or Problem
ACCORDING TO THE INFORMATION THESE TESTICULAR DEVICE WERE REMOVED DUE TO INFECTION.
Remedial action
- Other