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