FDA Adverse Event
Other
Summary report: N
PRIME BIG WHEEL STRETCHER, 30"
MDR report key: 2893218
·
Received December 21, 2012
Report
- Report Number
- 1831750-2012-13325
- Event Type
- Other
- Date Received
- December 21, 2012
- Date of Event
- September 30, 2012
- Report Date
- November 28, 2012
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FPO
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
MANUFACTURER'S INVESTIGATION IS STILL ONGOING; IF ADDITIONAL INFORMATION IS RECEIVED, A FOLLOW-UP REPORT MAY BE SUBMITTED.
Description of Event or Problem · 1
IT WAS REPORTED BY THE CUSTOMER THAT THE CUSTOMER (CAREGIVER) WAS ALLEGEDLY INJURED WHILE ATTEMPTING TO RELEASE THE STRETCHER BRAKE DURING PT TRANSFER. NO PT INJURY WAS RECORDED.
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 |