FDA Adverse Event
Malfunction
Summary report: N
CS BED 9153650455
MDR report key: 5003084
·
Received August 14, 2015
Report
- Report Number
- 1525712-2015-04273
- Event Type
- Malfunction
- Date Received
- August 14, 2015
- Date of Event
- July 16, 2015
- Report Date
- July 21, 2015
- Manufacturer
- FLEXTRONICS
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MD, US
- Reporter Occupation
- MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE
Narratives
Additional Manufacturer Narrative · 1
SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE A SUPPLEMENTAL RECORD WILL BE FILED.
Description of Event or Problem · 1
LOCKING MECHANISMS DID NOT WORK CORRECTLY AND BENT WHEN WE TRIED TO LOCK THE BED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 539506 | CS BED 9153650455 | BED, AC-POWERED ADJUSTABLE HOSPITAL | FNL | FLEXTRONICS | IHCS9FX |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |