FDA Adverse Event
Injury
Summary report: N
FERNO MODEL 93-H
MDR report key: 2992869
·
Received February 28, 2013
Report
- Report Number
- 1523574-2013-00001
- Event Type
- Injury
- Date Received
- February 28, 2013
- Date of Event
- January 19, 2013
- Report Date
- February 28, 2013
- Manufacturer
- FERNO-WASHINGTON, INC.
- Product Code
- FPO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- NOT APPLICABLE
Narratives
Additional Manufacturer Narrative · 1
USER FACILITY PURSUANT TO ITS INTERNAL PROCEDURES WILL NOT RELEASE ANY IDENTIFYING INFO RELATED TO ITS EMPLOYEE.
Description of Event or Problem · 1
EMT WAS INJURED WHEN STRETCHER DID NOT LOCK INTO PLACE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 87302 | FERNO MODEL 93-H | FERNO MODEL 93-H | FPO | FERNO-WASHINGTON, INC. | 93-H |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |