Device recall
Z-2652-2014: Tenor is a mobile passive lift, intended to be used on horizontal surfaces for…
FDA device recall · Class II · ARJOHUNTLEIGH POLSKA SP. ZO.O.
Key facts
| Recall number (Z-number) | Z-2652-2014 |
|---|---|
| Recall event | 68113 |
| Product | Tenor is a mobile passive lift, intended to be used on horizontal surfaces for lifting and transfer in hospitals, nursing homes or other healthcare facilities. Transfers with the Tenor are made indoors in the patient's room, in communal areas or in a bathroom. Tenor is meant to be used with the… |
| Product code | FSA |
| Recalling firm | ARJOHUNTLEIGH POLSKA SP. ZO.O. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 20, 2018 |
| 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