FDA Adverse Event
Malfunction
Summary report: N
TRANSPORT SERIES
MDR report key: 1915190
·
Received November 16, 2010
Report
- Report Number
- 1831750-2010-03854
- Event Type
- Malfunction
- Date Received
- November 16, 2010
- Date of Event
- October 4, 2010
- Report Date
- October 4, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV.
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FL, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
CONCLUSION: NO EVIDENCE OF LEAKING WAS OBSERVED.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD SECTION WAS DIFFICULT TO RAISE AND THE HYDRAULICS WERE LEAKING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | TRANSPORT SERIES | HOSPITAL WHEELED STRETCHER | FPO | STRYKER CORP., MEDICAL DIV. | 0721 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |