FDA Adverse Event Death Summary report: N

BREAST IMPLANTS

MDR report key: 480782 · Received August 24, 2003

Report

Report Number
MW1029367
Event Type
Death
Date Received
August 24, 2003
Date of Event
January 27, 1987
Report Date
August 24, 2003
Manufacturer
*
Product Code
FWM
Adverse Event
Yes
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
WA, US
Reporter Occupation
PATIENT FAMILY MEMBER OR FRIEND

Narratives

Description of Event or Problem · 1

PT DIED FROM RESPIRATORY FAILURE AFTER SUDDEN MYSTERIOUS CONDITION WHICH INCLUDED PNEUMONIA AND LUPUS, ALONG WITH MANY OTHER COMPLICATIONS THAT KILLED THEM WITHIN A YEAR. THEY HAD BREAST IMPLANTS IN THE MID 1970'S.

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 49 YR Death