FDA Adverse Event
Malfunction
Summary report: N
KNAPP IRIS SCISSORS 4" CURVED
MDR report key: 36111
·
Received August 2, 1996
Report
- Report Number
- 42933-1996-09001
- Event Type
- Malfunction
- Date Received
- August 2, 1996
- Manufacturer
- V. MUELLER DIV. BAXTER HEALTHCARE CORP
- Product Code
- HNF
- Report Source
- Manufacturer report
- Reporter Location
- AZ, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
THE ACCOUNT REPORTED THAT THE SCISSORS TIP BROKE OFF DURING A FACE LIFT OPERATION. THE ACCOUNT DOES NOT KNOW WHICH PHYSICIAN WAS INVOLVED, OR WHEN THE EVENT HAPPENED. ACCORDING TO THE ACCOUNT, THERE WAS NO PT INJURY AND NO MEDICAL OR SURGICAL INTERVENTION WAS REQUIRED AS A RESULT OF THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | KNAPP IRIS SCISSORS 4" CURVED | EYE SCISSORS | HNF | V. MUELLER DIV. BAXTER HEALTHCARE CORP | UNK | J |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |