FDA Enforcement Class II Ongoing

Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021

Recall: Z-1351-2019 · Reported May 22, 2019

Enforcement

Recall Number
Z-1351-2019
Event ID
81977
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Moller Vital
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
E-Mail
Report Date
May 22, 2019
Initiation Date
February 4, 2019
Classification Date
May 16, 2019
Address
Hadelandsvegen 2, P.o. Box 408, Gjovik, N/A, Norway

Description

Molift 2-Point sling bar, an accessory for Molift Mover 205. Item nos. 1430016 1430017 1430021

Reason

The firm has received 7 reports of malfunction for the device in which the hooks have broken off, potentially leading the sling to slip out of the sling bar and causing the patient to fall.

Code Info

All units manufactured between May 2013 and October 2018. Date of manufacture is labeled on the product.

Distribution

Domestic distribution to Arizona, Delaware, Florida, Georgia, Massachusetts, Ohio, South Carolina, Texas, Washington, and Wisconsin. Foreign distribution to Canada, Asia, Europe, and Australia.

Quantity

427 total