FDA Adverse Event Injury Summary report: N

SOFTFORM FACIAL IMPLANT

MDR report key: 189167 · Received September 25, 1998

Report

Report Number
2027148-1998-00078
Event Type
Injury
Date Received
September 25, 1998
Date of Event
August 1, 1998
Report Date
September 25, 1998
Manufacturer
TISSUE TECHNOLOGIES, INC.
Product Code
FTL
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

PT IMPLANTED IN UPPER VERMILION BORDERS 04/29/1998. ONSET OF INFECTION IN PERIORAL AREA 07/14/1998. IMPLANT EXPLANTED 08/1998.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SOFTFORM FACIAL IMPLANT Implant SOFTFORM FTL TISSUE TECHNOLOGIES, INC. NA UNK

Patients

Seq Age Sex Outcome Treatment
1 41 YR Required Intervention