Moller Vital: Medical Device Recall in 2019 - (Recall #: Z-1352-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Molift 2-Point sling bar, an accessory for Molift Mover 180/Air. Item nos. 1830001 1830002 1830002C 1830003

Product Classification:

Class II

Date Initiated: February 4, 2019

Date Posted: May 22, 2019

Recall Number: Z-1352-2019

Event ID: 81977

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 427 (total)

Code Information:

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

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated