Drug recall
Molift Air 205, Molift Air 205 Propulsion, Molift Air IRC, Molift Air 205 IRC Propulsion, Molift Air 300…
FDA recall event 74529 · Class II · Moller Vital
Key facts
| Event ID | 74529 |
|---|---|
| Recall numbers | Z-2291-2016 |
| Recalling firm | Moller Vital |
| Product type | Devices |
| Products | 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Potential for the bolt on the suspension coupling on the Molift Air to come loose from the housing. |
| Initiation date | Jun 24, 2016 |
| Report date | Aug 3, 2016 |
| Termination date | Jun 23, 2017 |
| City | Gjovik |
| Country | Norway |
| FEI number | 3004137175 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: