FDA Adverse Event
Injury
Summary report: N
STRYKER RENAISSANCE STRETCHER
MDR report key: 144784
·
Received January 9, 1998
Report
- Report Number
- 1831750-1998-00001
- Event Type
- Injury
- Date Received
- January 9, 1998
- Report Date
- January 7, 1998
- Manufacturer
- STRYKER CORP. MED. DIV.
- Product Code
- FPO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- NURSE
Narratives
Description of Event or Problem · 1
THREE EMPLOYEES HAVE ALLEGEDLY FRACTURED A FOOT RELEASING THE BRAKES ON A STRETCHER.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | STRYKER RENAISSANCE STRETCHER | HOSPITAL STRETCHER | FPO | STRYKER CORP. MED. DIV. | 1711 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | * | Required Intervention |