FDA Adverse Event
Other
Summary report: N
6083 AMBULANCE COT
MDR report key: 2003205
·
Received February 16, 2011
Report
- Report Number
- 1831750-2011-01425
- Event Type
- Other
- Date Received
- February 16, 2011
- Date of Event
- December 31, 2010
- Report Date
- January 19, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FPO
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
EVAL, RESULTS: HEIGHT ADJUSTMENT RACK; LITTER CROSS BRACE.
Description of Event or Problem · 1
IT WAS REPORTED THAT WHILE UNLOADING THE COT FROM THE AMBULANCE, THE COT LEGS DID NOT LOCK PROPERLY INTO POSITION. THE OPERATOR STOPPED THE COT FROM DROPPING. THE OPERATOR REPORTED HE HAS SINCE EXPERIENCED BACK PAIN AND STRAIN. NO INJURY TO THE (B)(6) PATIENT ONBOARD WAS ALLEGED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | 6083 AMBULANCE COT | STRETCHER, WHEELED | FPO | STRYKER MEDICAL | 6083 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |