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
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
- Reason category
- Device Malfunction
- Device type
- Other Medical Devices
Timeline
| 4 Feb 2019 | Recall initiated by company | |
| 16 May 2019 | Classified by FDA | +101 days |
| 22 May 2019 | Published 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.
More recalls from Moller Vital
All 5| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Molift 2-Point sling bar, an accessory for Molift Mover recalled | Moller Vital | Device Malfunction | 10 states |
| Device | CLASS II | Molift Air 300 IRC Propulsion Molift Air is a ceiling hoist recalled | Moller Vital | Foreign Material | Nationwide |
| Device | CLASS II | Molift Smart recalled by Moller Vital | Moller Vital | Device Malfunction | Nationwide |
| Device | CLASS II | Molift Smart recalled by Moller Vital | Moller Vital | Device Malfunction | Nationwide |
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