FDA Adverse Event
Other
Summary report: N
SECURE 3 MED/SURG BED
MDR report key: 1974561
·
Received January 20, 2011
Report
- Report Number
- 1831750-2011-00712
- Event Type
- Other
- Date Received
- January 20, 2011
- Date of Event
- December 13, 2010
- Report Date
- December 22, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MD, US
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
HEADBOARD. THE HEADBOARD WAS REPLACED.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE BEDS WERE DELIVERED ON (B)(6) AND PLACED INTO A BRAND NEW, UNOPENED PT CARE UNIT. WHEN (B)(6) INSPECTED THE BEDS, HE FOUND THE DAMAGE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | SECURE 3 MED/SURG BED | AC POWERED HOSPITAL BED | FNL | STRYKER CORP., MEDICAL DIV. | 3002S3 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |