FDA Adverse Event
Other
Summary report: N
COR21000262-000
MDR report key: 12377554
·
Received August 27, 2021
Report
- Report Number
- COR21000262-000
- Event Type
- Other
- Date Received
- August 27, 2021
- Report Date
- August 26, 2021
- Manufacturer
- Leidos, Inc
- Product Code
- RCE
- Report Source
- Manufacturer report
- Reporter Location
- MA, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1273144 | RCE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |