FDA Adverse Event
Malfunction
Summary report: N
NASAL SNARE WIRE
MDR report key: 435285
·
Received December 24, 2002
Report
- Report Number
- 2515651-2002-00010
- Event Type
- Malfunction
- Date Received
- December 24, 2002
- Manufacturer
- KARL AUGUST HUBER GMBH
- Product Code
- KBE
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- INVALID DATA
Narratives
Description of Event or Problem · 1
THE USER FACILITY REPORTED THAT A NASAL SNARE WIRE BROKE INTRAOPERATIVELY. NO INJURIES WERE REPORTED DUE TO THIS INCIDENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | NASAL SNARE WIRE | NASAL SNARE WIRE, 8 GAUGE, THROAT | KBE | KARL AUGUST HUBER GMBH | * | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |