FDA Adverse Event
Malfunction
Summary report: N
JET CIRCUIT
MDR report key: 556352
·
Received August 25, 2004
Report
- Report Number
- MW1033056
- Event Type
- Malfunction
- Date Received
- August 25, 2004
- Date of Event
- August 23, 2004
- Report Date
- August 24, 2004
- Manufacturer
- BUNNELL INC.
- Product Code
- BZO
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- TX, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
TUBING WAS DETACHED FROM PRODUCT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | JET CIRCUIT | JET CIRCUIT | BZO | BUNNELL INC. | * | 4D0148 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Other |