FDA Adverse Event
Malfunction
Summary report: N
FOGARTY HUDRAGRIP CLAMP
MDR report key: 70776
·
Received February 20, 1997
Report
- Report Number
- 1423537-1997-00031
- Event Type
- Malfunction
- Date Received
- February 20, 1997
- Report Date
- February 18, 1997
- Manufacturer
- STE - 1923569 - V. MUELLER/SURGICAL GROUP
- Product Code
- DXC
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
THE JAW ON THE CLAMP CRACKED WHILE IN USE ON A SURGICAL PROCEDURE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | FOGARTY HUDRAGRIP CLAMP | VASCULAR CLAMP | DXC | STE - 1923569 - V. MUELLER/SURGICAL GROUP | CV5050 | HB |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNKNOWN | Other |