FDA Adverse Event
Malfunction
Summary report: N
EYE SURGERY STRETCHER
MDR report key: 2222496
·
Received July 13, 2011
Report
- Report Number
- 1831750-2011-07033
- Event Type
- Malfunction
- Date Received
- July 13, 2011
- Date of Event
- June 7, 2011
- Report Date
- June 15, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- FPO
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- FR
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
EVAL RESULT: HEADREST.
Description of Event or Problem · 1
IT WAS REPORTED IN A SERVICE REPORT THAT DURING INSPECTION OF THE DEVICE, THE LOCKING SYSTEM OF THE HEADREST COULD NOT BE LOCKED IN PLACE. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | EYE SURGERY STRETCHER | HOSPITAL WHEELED STRETCHER | FPO | STRYKER MEDICAL | 1089 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |