FDA Adverse Event Injury Summary report: N

SMOOTH SALINE-FILLED MAMMARY PROSTHESIS

MDR report key: 5998035 · Received October 4, 2016

Report

Report Number
1645337-2016-00134
Event Type
Injury
Date Received
October 4, 2016
Date of Event
September 1, 2014
Report Date
November 28, 2016
Manufacturer
MENTOR WW LLC
Product Code
FWM
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

ACCORDING TO THE INFORMATION PROVIDED, THE PATIENT EXPERIENCED AUTOIMMUNE SYMPTOMS "THE PATIENT EXPERIENCED DIFFICULTY FOCUSING "BRAIN FOG" AND WANTED IMPLANTS REMOVED. NO SUPPORTING DOCUMENTATION WAS PROVIDED BY A HEALTH AUTHORITY OFFICIAL. NO SUPPORTING DOCUMENTATION WAS PROVIDED BY A HEALTH AUTHORITY OFFICIAL. PRODUCT EVALUATION RECEIVED TWO UNLABELED DEVICES. DEVICE "A" WAS RETURNED EMPTY OF FLUID. UPON RECEIPT BY MENTOR, THE CONTRALATERAL DEVICE WEIGHED 29.3 GRAMS. BASED ON THE LABORATORY EVALUATIONS, THE DEVICES APPEARED INTACT WITH NO ANOMALIES. DUE TO THE NATURE OF THE COMPLAINTS, PE WAS PRECLUDED FROM FURTHER EVALUATING THE DEVICE. CONCERN OVER THE ASSOCIATION OF BREAST IMPLANTS TO THE DEVELOPMENT OF AUTOIMMUNE OR CONNECTIVE TISSUE DISEASES, SUCH AS LUPUS, SCLERODERMA, OR RHEUMATOID ARTHRITIS, WAS RAISED BECAUSE OF CASES REPORTED IN LITERATURE WITH SMALL NUMBERS OF WOMEN WITH IMPLANTS. SCIENTIFIC EXPERT PANELS AND LITERATURE REPORTS HAVE FOUND NO EVIDENCE OF A CONSISTENT PATTERN OF SIGNS AND SYMPTOMS ASSOCIATED WITH THESE DISEASES IN WOMEN WITH BREAST IMPLANTS. ADDITIONALLY, HAVING RHEUMATOLOGICAL SIGNS AND SYMPTOMS DOES NOT NECESSARILY MEAN A PATIENT HAS A CONNECTIVE TISSUE DISORDER OR AUTOIMMUNE DISEASE. PER THE FDA'S "UPDATE ON THE SAFETY OF SILICONE GEL-FILLED BREAST IMPLANTS" PUBLISHED IN JUNE 2011, "THERE IS NO APPARENT ASSOCIATION BETWEEN SILICONE GEL-FILLED BREAST IMPLANTS AND CONNECTIVE TISSUE DISEASE, BREAST CANCER, OR REPRODUCTIVE PROBLEMS." FURTHERMORE, THE (B)(6) RELEASED A FINAL REPORT STATING "A REVIEW OF SEVENTEEN EPIDEMIOLOGICAL REPORTS OF CONNECTIVE TISSUE DISEASE IN WOMEN WITH BREAST IMPLANTS WAS REMARKABLE FOR ITS CONSISTENCY IN FINDING NO ELEVATED RISKS OR ODDS RATIO FOR AN ASSOCIATION OF IMPLANTS WITH DISEASE[?] THERE IS NO EVIDENCE THAT SILICONE IMPLANTS ARE RESPONSIBLE FOR ANY MAJOR DISEASES OF THE WHOLE BODY. WOMEN ARE EXPOSED TO SILICONE CONSTANTLY IN THEIR DAILY LIVES. THERE IS NO PLAUSIBLE EVIDENCE OF A NOVEL AUTOIMMUNE.

Description of Event or Problem · 1

AUTOIMMUNE SYMPTOMS: DIFFICULTY FOCUSING "BRAIN FOG".

Description of Event or Problem · 1

AUTO IMMUNE SYMPTOMS. BRAIN FOG.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
648581 SMOOTH SALINE-FILLED MAMMARY PROSTHESIS BREAST IMPLANT FWM MENTOR WW LLC 350-3420

Patients

Seq Age Sex Outcome Treatment
1 37 YR Other