CLASS II ONGOING Device recall · Reported 22 May 2019 · FDA Enforcement Report

Molift 2-Point sling bar, an accessory for Molift Mover 180/Air recalled

Moller Vital is recalling Molift 2-Point sling bar, an accessory for Molift Mover 180/Air, distributed in 10 states. The recall was initiated on 4 Feb 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll units manufactured between May 2013 and October 2018. Date of manufacture is labeled on the product.
Quantity recalled427 (total)

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1352-2019
FDA event ID
81977
Recalling firm
Moller Vital, Gjovik
Classification
Class II
Status
Ongoing
Recall initiated
4 Feb 2019
FDA classified
16 May 2019
Reported
22 May 2019
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Device Malfunction

Timeline

4 Feb 2019Recall initiated by company
16 May 2019Classified by FDA+101 days
22 May 2019Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

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.

Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.

Product as listed by the FDA

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

Where it was distributed

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

ArizonaDelawareFloridaGeorgiaMassachusettsOhioSouth CarolinaTexasWashingtonWisconsin

Questions about this recall

Is Molift 2-Point sling bar, an accessory for Molift Mover 180/Air recalled?

Yes. Moller Vital recalled Molift 2-Point sling bar, an accessory for Molift Mover 180/Air on 4 Feb 2019. The recall is Class II and its status is Ongoing. Recall number Z-1352-2019.

Why was it recalled?

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.

Which lots are affected?

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

Where was it sold?

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

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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