FDA Adverse Event
Other
Summary report: N
MITY VAC
MDR report key: 1221862
·
Received July 7, 2008
Report
- Report Number
- 1216677-2008-00021
- Event Type
- Other
- Date Received
- July 7, 2008
- Date of Event
- January 8, 2008
- Report Date
- July 7, 2008
- Manufacturer
- COOPERSURGICAL, INC.
- Product Code
- HDB
- Report Source
- Manufacturer report
Narratives
Additional Manufacturer Narrative · 0
LOT INFO IS NOT AVAILABLE. THE VACUUM SOURCE HAS NOT BEEN IDENTIFIED. SUPPLEMENTAL INFO WILL BE PROVIDED SHOULD ANY FURTHER INVESTIGATION BE POSSIBLE. (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 0 | MITY VAC | EXTRACTOR CUP | HDB | COOPERSURGICAL, INC. | 10007LP | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 0 | Other |