FDA Adverse Event
Injury
Summary report: N
PELVICOL ACELLULAR COLLAGEN MATRIX 4X7 CM
MDR report key: 3143022
·
Received May 24, 2013
Report
- Report Number
- 9617613-2013-00300
- Event Type
- Injury
- Date Received
- May 24, 2013
- Date of Event
- June 30, 2004
- Report Date
- April 4, 2018
- Manufacturer
- COVIDIEN, FORMERLY TISSUE
- Product Code
- FTL
- PMA / PMN Number
- K992556
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- OTHER
- Health Professional
- N
Narratives
Additional Manufacturer Narrative · 1
(B)(4).
Description of Event or Problem · 1
PROCEDURE TYPE: STRESS UI/ PELVIC ORGAN PROLAPSE. ACCORDING TO THE REPORTER: THE PATIENT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. PRODUCT WAS USED FOR THERAPEUTIC TREATMENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 231589 | PELVICOL ACELLULAR COLLAGEN MATRIX 4X7 CM | PELVICOL MESH | FTL | COVIDIEN, FORMERLY TISSUE | 04B03-1 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 35 YR | Female | Other | EXP: 04/30/2013.| URETEX SUPPORT PP KIT X1: LOT # C24012SUP.| URETEXSUP.| URETEXSUP| URETEX SUPPORT PP KIT X1: LOT # C24012SUP| EXP: 04/30/2013 |