Device recall
Z-1811-2026: Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US
FDA device recall · Class II · ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Key facts
| Recall number (Z-number) | Z-1811-2026 |
|---|---|
| Recall event | 98542 |
| Product | Arjo Tenor mobile passive patient lift, Model Numbers KHA1000 US and KHA1010 US |
| Product code | FSA |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3007420694 |
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