Device recall
Z-2753-2018: Handicare P600 Series Patient Lift Product Usage: A device used to lift and…
FDA device recall · Class II · Handicare Usa Inc
Key facts
| Recall number (Z-number) | Z-2753-2018 |
|---|---|
| Recall event | 80556 |
| Product | Handicare P600 Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another. |
| Product code | FNL |
| Recalling firm | Handicare Usa Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 10, 2020 |
| FEI number | 3007802293 |
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