FDA Adverse Event
Injury
Summary report: N
BRAND
MDR report key: 7749745
·
Received August 5, 2018
Report
- Report Number
- MW5078862
- Event Type
- Injury
- Date Received
- August 5, 2018
- Product Code
- DFD
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
TEST B5
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 591792 | BRAND | TD | DFD |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Life Threatening | TEST |