Device recall
Z-2693-2014: Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended…
FDA device recall · Class II · ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Key facts
| Recall number (Z-number) | Z-2693-2014 |
|---|---|
| Recall event | 68594 |
| Product | Minstrel (with scale) Product Usage: is a mobile passive hoist. It is intended for lifting and transporting adult residents on horizontal floors in hospitals, nursing homes or other health care facilitates. The Minstrel device aids in the lifting, transfer and lowering to safe position, of a… |
| Product code | FSA |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 13, 2016 |
| 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