FDA Adverse Event
Malfunction
Summary report: N
GYNNIE OB-GYN STRETCHER
MDR report key: 2091235
·
Received April 20, 2011
Report
- Report Number
- 1831750-2011-03847
- Event Type
- Malfunction
- Date Received
- April 20, 2011
- Date of Event
- March 23, 2011
- Report Date
- March 23, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- HDD
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
EVALUATION: BUMPER CHANNEL.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE BUMPER CHANNEL WAS DAMAGED PRESENTING SHARP EXPOSED EDGES. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GYNNIE OB-GYN STRETCHER | HOSPITAL WHEELED STRETCHER | HDD | STRYKER MEDICAL | 1061 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA |