FDA Adverse Event
Malfunction
Summary report: N
COR18000015-000
MDR report key: 7187866
·
Received January 12, 2018
Report
- Report Number
- COR18000015-000
- Event Type
- Malfunction
- Date Received
- January 12, 2018
- Report Date
- January 11, 2018
- Product Code
- RCG
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- OTHER
- Health Professional
- I
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 28624 | RCG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |