Device recall
Z-1486-2024: Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg…
FDA device recall · Class II · Human Care Hc Sweden Ab
Key facts
| Recall number (Z-number) | Z-1486-2024 |
|---|---|
| Recall event | 94140 |
| Product | Altair 330 lbs w/o Hanger Bar, REF: 55200H-NA, 55220H-NA, and Roomer S 220 kg w/o Hanger Bar, REF: 55300H-NA, patient lifts |
| Product code | FSA |
| Recalling firm | Human Care Hc Sweden Ab |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3006291016 |
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