FDA Adverse Event
Injury
Summary report: N
GYNECARE TVT SECUR SYSTEM
MDR report key: 3202006
·
Received July 2, 2013
Report
- Report Number
- 2210968-2013-11890
- Event Type
- Injury
- Date Received
- July 2, 2013
- Report Date
- June 27, 2013
- Manufacturer
- ETHICON INC.
- Product Code
- PAH
- PMA / PMN Number
- K052401
- Removal / Correction Number
- NA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
(B)(4). NO CONCLUSION CAN BE DRAWN AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE OBTAINED, A SUPPLEMENTAL 3500A FORM WILL BE SUBMITTED ACCORDINGLY.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE PATIENT UNDERWENT A GYNECOLOGICAL PROCEDURE ON (B)(6) 2008 AND MESH WAS IMPLANTED. THERE IS MENTION OF PROCEDURES ON (B)(6) 2012 AND (B)(6) 2013. NO CLARIFYING INFORMATION PROVIDED. IT IS ALSO REPORTED THAT THE PATIENT EXPERIENCED PAIN, EROSION OF INTERNAL TISSUES, AND HAS UNDERGONE ADDITIONAL SURGERIES AND REVISIONARY PROCEDURES.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 302151 | GYNECARE TVT SECUR SYSTEM | MESH, SURGICAL, SYNTHETIC, UROGYNECOLOGIC | PAH | ETHICON INC. | UNK | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Required Intervention |