FDA Adverse Event
Malfunction
Summary report: N
LD304 MATERNITY BED
MDR report key: 2000245
·
Received February 3, 2011
Report
- Report Number
- 1831750-2011-01022
- Event Type
- Malfunction
- Date Received
- February 3, 2011
- Date of Event
- January 7, 2011
- Report Date
- January 7, 2011
- Manufacturer
- STRYKER MEDICAL
- Product Code
- HDD
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NY, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
LEFT CALF SUPPORT.
Description of Event or Problem · 1
IT WAS REPORTED BY SERVICE REPORT THAT THE CALF SUPPORT IS CRACKED. THE CUSTOMER DID NOT KNOW IF THERE WAS PATIENT INVOLVEMENT OF AN ALLEGED INJURY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | LD304 MATERNITY BED | LABOR AND DELIVERY BED | HDD | STRYKER MEDICAL | 4701 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |