Device recall
Z-0549-2019: Invacare 9805 and 9805P Hydraulic Patient Lifts, Model Nos. 9805 and 9805P The…
FDA device recall · Class II · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-0549-2019 |
|---|---|
| Recall event | 81071 |
| Product | 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 bed to a wheelchair. The device includes straps and a sling to support the patient. |
| Product code | FSA |
| Recalling firm | Invacare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 15, 2020 |
| FEI number | 1525712 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database