FDA Adverse Event
Malfunction
Summary report: N
CAREASSIST BED
MDR report key: 3023085
·
Received February 27, 2013
Report
- Report Number
- 9615739-2013-00055
- Event Type
- Malfunction
- Date Received
- February 27, 2013
- Date of Event
- January 31, 2013
- Report Date
- January 31, 2013
- Manufacturer
- HILL-ROM PLUVIGNER
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TW
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
THE ACCOUNT STATED THAT THEY INSPECTED THE CARDIO PULMONARY RESUSCITATION CABLE AND FOUND RUST ON THE CABLE WHERE IT CONNECTS TO THE CARDIO PULMONARY RESUSCITATION PULL HANDLE. NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.
Description of Event or Problem · 1
THE ACCOUNT ALLEGED THAT THE CARDIO PULMONARY RESUSCITATION IS NOT FUNCTIONING. NO PATIENT IMPACT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 85150 | CAREASSIST BED | A/C POWERED ADJUSTABLE HOSPITAL BED | FNL | HILL-ROM PLUVIGNER | 1170 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |