Drug recall
Invacare 9805 and 9805P Hydraulic Patient Lifts, Model Nos. 9805 and 9805P The intended use of a…
FDA recall event 81071 · Class II · Invacare Corporation
Key facts
| Event ID | 81071 |
|---|---|
| Recall numbers | Z-0549-2019 |
| Recalling firm | Invacare Corporation |
| Product type | Devices |
| Products | Invacare 9805 and 9805P Hydraulic Patient Lifts, Model Nos. 9805 and 9805P The intended use of a Non-AC-Powered patient lift is to lift and transfer a patient from one surface to another, as from a… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Invacare has identified via customer complaints, the potential for the mounting bolt connecting the caster to the base frame of the patient lifts to become loose. Loose hardware can cause wear to the… |
| Initiation date | Nov 16, 2018 |
| Report date | Dec 12, 2018 |
| Termination date | Apr 15, 2020 |
| City | Elyria |
| State | OH |
| Country | United States |
| FEI number | 1525712 |
At a glance
- 1–9 Products in this recall
- 10–99 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: