FDA Adverse Event
Summary report: N
*
MDR report key: 1083458
·
Received July 29, 2008
Report
- Report Number
- MW5007814
- Date Received
- July 29, 2008
- Date of Event
- July 29, 2002
- Report Date
- July 29, 2008
- Product Code
- FMF
- Report Source
- Voluntary report
- Reporter Location
- PA, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
PRODUCTS RECALL BD 60 ML SYRINGE LOT # 6117415 REORDER # 309653 QUESTIONABLE PRODUCT STERILITY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | * | NONE | FMF | 6117415 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * |