FDA Adverse Event Injury Summary report: N

SOFTFORM FACIAL IMPLANT

MDR report key: 288637 · Received August 4, 2000

Report

Report Number
2027148-2000-00040
Event Type
Injury
Date Received
August 4, 2000
Date of Event
March 20, 2000
Report Date
August 4, 2000
Manufacturer
TISSUE TECHNOLOGIES, INC.
Product Code
FTL
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

PT IMPLANTED IN NASOLABIAL FOLDS, DATE UNKNOWN. ONSET OF INFECTION IN 2000. PT TREATED WITH ANTIBIOTICS IN 2000.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SOFTFORM FACIAL IMPLANT SOFTFORM FTL TISSUE TECHNOLOGIES, INC. NA K04888/00A371

Patients

Seq Age Sex Outcome Treatment
1 NO INFO Required Intervention