FDA Adverse Event
Malfunction
Summary report: N
GOBED+
MDR report key: 1942699
·
Received December 10, 2010
Report
- Report Number
- 1831750-2010-04724
- Event Type
- Malfunction
- Date Received
- December 10, 2010
- Date of Event
- November 12, 2010
- Report Date
- November 12, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIVISION
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IA, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
NURSE CALL CORD.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE RECEPTACLE FOR THE NURSE CALL CORD WAS BROKEN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | GOBED+ | IMPLANT | FNL | STRYKER CORP., MEDICAL DIVISION | FL20E | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |