FDA Adverse Event
Injury
Summary report: N
PRIME BIG WHEEL STRETCHER, 30"
MDR report key: 2112320
·
Received May 24, 2011
Report
- Report Number
- 1831750-2011-04976
- Event Type
- Injury
- Date Received
- May 24, 2011
- Date of Event
- April 25, 2011
- Report Date
- April 25, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FPO
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
EVALUATION IS IN PROCESS. A FOLLOW-UP REPORT WILL BE FILED UPON COMPLETION OF THE EVALUATION.
Description of Event or Problem · 1
IT WAS REPORTED THAT A NURSE HAS BEEN INJURED OVER TIME WHILE TRYING TO PUT THE BIG WHEEL INTO STEER MODE USING THE SIDE CONTROLS. SHE HAS BEEN REQUIRED TO WEAR AN ANKLE BOOT. THE REPORTER STATES THAT THE AMOUNT OF FORCE TO OPERATE IS SIGNIFICANTLY GREATER THAN THE STRETCHERS OF THE SAME MODEL THAT THEY HAVE IN HOUSE. THIS STRETCHER REMAINS IN SERVICE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | PRIME BIG WHEEL STRETCHER, 30" | HOSPITAL WHEELED STRETCHER | FPO | STRYKER MEDICAL | 1115000030 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |