CUI SMOOTH SILICONE GEL FILLED BREAST IMPLANT
Report
- Report Number
- 9617229-2023-06989
- Event Type
- Injury
- Date Received
- April 19, 2023
- Date of Event
- August 1, 2022
- Report Date
- December 18, 2023
- Manufacturer
- ALLERGAN (COSTA RICA)
- Product Code
- FTR
- UDI-DI
- 05060191609111
- PMA / PMN Number
- P020056
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- US
- Reporter Occupation
- OTHER
- Health Professional
- N
Narratives
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: RUPTURE.
A REVIEW OF THE DEVICE HISTORY RECORD HAS BEEN COMPLETED. NO DEVIATIONS OR NON-CONFORMANCES NOTED. TWO DEVICE REPORTED. UNKNOWN WHAT SIDE EACH DEVICE IS AND WHAT SIDE THE COMPLAINTS ARE FOR. SN (B)(6)/LOT 3052151/ CATALOG C-SHD-340. SN (B)(6)/LOT 3076172/CATALOG C-SHD-340.
PATIENT REPORTED LEFT SIDE "ANXIETY", "TENDERNESS, HURT", "WEAKNESS" (NON DEVICE RELATED), AND "PHYSICIAN RECOMMENDED AN ULTRASOUND TO CONFIRM A RUPTURE". THE DEVICE REMAINS IMPLANTED.
PATIENT REPORTED LEFT SIDE "ANXIETY", "TENDERNESS, HURT", "WEAKNESS" (NON DEVICE RELATED), AND "PHYSICIAN RECOMMENDED AN ULTRASOUND TO CONFIRM A RUPTURE". THE DEVICE REMAINS IMPLANTED.
PATIENT REPORTED UNKNOWN SIDE "ANXIETY", "TENDERNESS, HURT", "WEAKNESS" (NON DEVICE RELATED), AND "PHYSICIAN RECOMMENDED AN ULTRASOUND TO CONFIRM A RUPTURE". THE DEVICE REMAINS IMPLANTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1685705 | CUI SMOOTH SILICONE GEL FILLED BREAST IMPLANT | PROSTHESIS, BREAST, NONINFLATABLE, INTERNAL, SILICONE GEL-FILLED | FTR | ALLERGAN (COSTA RICA) | 3076172 | 05060191609111 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 27 YR | Female | Required Intervention |