FDA Adverse Event
Malfunction
Summary report: N
LINET
MDR report key: 7078643
·
Received December 1, 2017
Report
- Report Number
- MW5073683
- Event Type
- Malfunction
- Date Received
- December 1, 2017
- Report Date
- November 29, 2017
- Manufacturer
- LINET AMERICAS
- Product Code
- FNL
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- MS, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
Narratives
Description of Event or Problem · 1
WELD IS CRACKING IN THE SAME PLACE ON 17 OUT OF 20 ICU BEDS AT THE MEDICAL CENTER. THE WELD LOCATION IS AT A POINT THAT ATTACHES THE KNEE-LIFT ACTUATOR MOTOR BRACKET TO THE FRAME. THIS CAUSES THE MOTOR TO DROP LOWER. SOME ARE CRACKING WORSE THAN OTHERS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 853952 | LINET | LINET MULTICARE BED | FNL | LINET AMERICAS | MULTICARE |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |