FDA Adverse Event
Malfunction
Summary report: N
ZOOM CRITICAL CARE BED
MDR report key: 1694156
·
Received May 14, 2010
Report
- Report Number
- 1831750-2010-00980
- Event Type
- Malfunction
- Date Received
- May 14, 2010
- Date of Event
- April 21, 2010
- Report Date
- April 21, 2010
- Manufacturer
- STRYKER CORP., MEDICAL DIV.
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- WV, US
- Reporter Occupation
- UNKNOWN
Narratives
Additional Manufacturer Narrative · 1
FOOTBOARD. IT WAS REPORTED TO THE SALES REP BY THE USER FACILITY THAT PTS HAD BEEN KICKING THE FOOTBOARD, BREAKING THEM STRUCTURALLY AND ELECTRONICALLY.
Description of Event or Problem · 1
IT WAS REPORTED THAT THE FOOTBOARD WAS BROKEN. NO ADVERSE CONSEQUENCES ALLEGED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ZOOM CRITICAL CARE BED | A/C POWERED HOSPITAL BED | FNL | STRYKER CORP., MEDICAL DIV. | 2040 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | UNK |