FDA Adverse Event
Malfunction
Summary report: N
JAKO-KLEINSASSER MICRO-LARYNGEAL SCISSORS
MDR report key: 613756
·
Received July 12, 2004
Report
- Report Number
- 2515651-2004-00004
- Event Type
- Malfunction
- Date Received
- July 12, 2004
- Report Date
- June 11, 2004
- Manufacturer
- *
- Product Code
- KBM
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- PA, US
- Reporter Occupation
- OTHER
Narratives
Description of Event or Problem · 1
A SMALL PIECE OF THE SCISSOR'S BLADE DETACHED FROM THE INSTRUMENT DURING A MICRO DIRECT LARYNGOSCOPY PROCEDURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | JAKO-KLEINSASSER MICRO-LARYNGEAL SCISSORS | MICRO-LARYNGEAL SCISSORS | KBM | * | * | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |