FDA Adverse Event
Malfunction
Summary report: N
COR17000706-000
MDR report key: 6839137
·
Received September 1, 2017
Report
- Report Number
- COR17000706-000
- Event Type
- Malfunction
- Date Received
- September 1, 2017
- Report Date
- August 31, 2017
- Manufacturer
- L3 Technologies, Inc
- 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 |
|---|---|---|---|---|---|---|---|
| 617060 | RCG |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |