FDA Adverse Event Injury Summary report: N

MENTOR

MDR report key: 1080847 · Received July 22, 2008

Report

Report Number
MW5007750
Event Type
Injury
Date Received
July 22, 2008
Date of Event
July 21, 2008
Report Date
July 22, 2008
Product Code
FWM
Adverse Event
Yes
Report Source
Voluntary report
Reporter Location
NV, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

BILATERAL REMOVE AND REPLACE BREAST IMPLANTS. LEFT BREAST RUPTURED. BILATERAL CAPSULE CONTRACTURES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MENTOR BREAST IMPLANTS FWM UNK

Patients

Seq Age Sex Outcome Treatment
1 42 YR