FDA Adverse Event
Injury
Summary report: N
STAIR PRO - MODEL 6252
MDR report key: 1971467
·
Received January 19, 2011
Report
- Report Number
- 1831750-2011-00680
- Event Type
- Injury
- Date Received
- January 19, 2011
- Date of Event
- December 21, 2010
- Report Date
- December 22, 2010
- Manufacturer
- STRYKER CORP, MEDICAL DIV.
- Product Code
- FPO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- UNKNOWN
Narratives
Description of Event or Problem · 1
IT WAS REPORTED BY PHONE THAT THE TRACK ON THE RIGHT SIDE OF THE CHAIR WAS NOT LATCHED AND STARTED BOWING DURING USE AND THE EMT WAS NOT ABLE TO CONTROL THE CHAIR. THERE WAS A PT ON THE CHAIR AT THE TIME OF THE INCIDENT. THE CHAIR AND THE PT FELL DOWN APPROX 8 STAIRS WHICH CAUSED THE EMT TO SUFFER FROM VARIOUS BRUISING AND THE PT TO SUFFER FROM A BLOODY LIP AND AN ABRASION TO THE KNEE. THERE WAS BOTH PT INVOLVEMENT AND ADVERSE CONSEQUENCES REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | STAIR PRO - MODEL 6252 | STRETCHER, HAND-CARRIED | FPO | STRYKER CORP, MEDICAL DIV. | 6252 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 55 YR | Other |