FDA Adverse Event
Malfunction
Summary report: N
KINSA SUTURE ANCHOR SYSTEM, MACHINED PEEK
MDR report key: 1000752
·
Received February 19, 2008
Report
- Report Number
- 1219602-2008-00023
- Event Type
- Malfunction
- Date Received
- February 19, 2008
- Report Date
- June 18, 2007
- Manufacturer
- SMITH & NEPHEW INC., ENDOSCOPY DIV.
- Product Code
- MBI
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- OTHER
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KINSA SUTURE ANCHOR SYSTEM, MACHINED PEEK | KINSA SUTURE ANCHOR | MBI | SMITH & NEPHEW INC., ENDOSCOPY DIV. | 72200743 | 50183989 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |