FDA Adverse Event
Summary report: N
N/A
MDR report key: 3621540
·
Received January 28, 2014
Report
- Report Number
- 3621540
- Date Received
- January 28, 2014
- Date of Event
- January 23, 2014
- Report Date
- January 28, 2014
- Manufacturer
- CAREFUSION 213 LLC
- Product Code
- LWK
- Report Source
- User Facility report
- Reporter Location
- CA, US
- Reporter Occupation
- RISK MANAGER
Narratives
Description of Event or Problem · 1
BILATERAL GROINS WERE BEING CLIPPED, AND CAUSED ABRASIONS AND REDDENED SKIN.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 61299 | N/A | RAZOR, SURGICAL | LWK | CAREFUSION 213 LLC | CF27-101 | * |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 70 YR |