Molift Air 205 — Class II medical device recall Z-2291-2016
Terminated recall by Moller Vital, reported 2016-08-03, distributed nationwide. Potential for the bolt on the suspension coupling on the Molift Air to come loose from the housing.
| Recall number | Z-2291-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Moller Vital, Gjovik, N/A, Norway |
| Recall initiated | 2016-06-24 |
| Classified | 2016-07-26 |
| Reported by FDA | 2016-08-03 |
| Terminated | 2017-06-23 |
| Distributed | Nationwide (US) |
Product
Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC Propulsion, Molift Air 300, Molift Air 300 Propulsion, Molift Air 300 IRC, Molift Air 300 IRC Propulsion Molift Air is a ceiling hoist used to lift and transfer immobilized patients in various situations. The coupling that holds the suspension is fixed to the lifting belt by a bolt through an aluminum housing. The bolt is hold in place by a rubber cap secured with a small screw. The other end of the lifting belt is fixed to the lifting drum on the motor. The design is identical on both Air 205 and Air 300 in all variants
Reason for recall
Potential for the bolt on the suspension coupling on the Molift Air to come loose from the housing.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2291-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.