UNK MAMMARY IMPLANT
Report
- Report Number
- 9617229-2025-20294
- Event Type
- Injury
- Date Received
- November 21, 2025
- Date of Event
- April 1, 2020
- Report Date
- November 21, 2025
- Manufacturer
- ALLERGAN (COSTA RICA)
- Product Code
- FWM
- PMA / PMN Number
- P990074
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- 003
Narratives
THE EVENT OF "CAPSULAR CONTRACTURE" IS A PHYSIOLOGICAL COMPLICATION AND ANALYSIS OF THE DEVICE GENERALLY DOES NOT ASSIST ALLERGAN IN DETERMINING A PROBABLE CAUSE FOR THIS EVENT. FURTHER INFORMATION FROM THE REPORTER REGARDING EVENT, PRODUCT, OR PATIENT DETAILS HAS BEEN REQUESTED. NO ADDITIONAL INFORMATION IS AVAILABLE AT THIS TIME. REASON FOR REOPERATION: CAPSULAR CONTRACTURE, BAKER GRADE UNKNOWN AND SILICONE MIGRATION.
PATIENT REPORTED ¿INCREASING CADENCE IN FLARE-UPS, INCLUDING SWELLING IN BOTH BREASTS¿, ¿HOT/BURNING FEELING¿, ¿GENERAL FEELING OF MALAISE¿, ¿BACK AND UNDER BREAST CRAMPING¿, ¿RESULTING IN BOTH IMPLANTS COMPLETELY CAPSULATED AND POTENTIALLY FIXED TO CHEST WALL¿. PATIENT LATER REPORTED "I AM NOW ALSO BEING INVESTIGATED FOR WHAT IS LIKELY A RETURN OF MY BREAST CANCER, ALSO IN MY LIVER AND POSSIBLY LUNG. I HAVE ALSO DEVELOPED SOME KIND OF SEVERE AUTO-IMMUNE DISEASE, PARTICULARLY IN CONTACT WITH PLASTICS, CT SCANS ALSO SHOW THAT I HAVE LYMPH NODES THAT APPEAR TO STILL HAVE SILICON". THIS RECORD IS FOR THE RIGHT SIDE. DEVICE HAS BEEN EXPLANTED. DEVICE RETURN UNKNOWN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2303947 | UNK MAMMARY IMPLANT | PROSTHESIS, BREAST, INFLATABLE, INTERNAL, SALINE | FWM | ALLERGAN (COSTA RICA) | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 39 YR | Female | Required Intervention |