FDA Adverse Event
Malfunction
Summary report: N
LD304 MATERNITY BED
MDR report key: 1915223
·
Received November 16, 2010
Report
- Report Number
- 1831750-2010-03893
- Event Type
- Malfunction
- Date Received
- November 16, 2010
- Date of Event
- October 19, 2010
- Report Date
- October 19, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV.
- Product Code
- HDD
- PMA / PMN Number
- KP50889
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- AL, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
RESULT: TREND SWITCH BRACKET.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END IS TOO LOW WHEN BED IS AT LOWEST POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LD304 MATERNITY BED | LABOR AND DELIVERY BED | HDD | STRYKER CORP., MEDICAL DIV. | 4701 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |