FDA Adverse Event
Other
Summary report: N
9610617-2009-00003
MDR report key: 1325109
·
Received January 27, 2009
Report
- Report Number
- 9610617-2009-00003
- Event Type
- Other
- Date Received
- January 27, 2009
- Product Code
- HET
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 1
MOTOR WAS TESTED WITH CONTROL UNIT AND TECHNICIAN COULD NOT DUPLICATE ALLEGED PROBLEM. NO ERROR MESSAGES RECEIVED. ROUTINE MAINTENANCE CONDUCTED ON CONTROL UNIT AND FUSES WERE REPLACED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | HET |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |