Device recall
Z-0589-2019: ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage: The Arjo…
FDA device recall · Class II · ARJOHUNTLEIGH POLSKA Sp. z.o.o.
Key facts
| Recall number (Z-number) | Z-0589-2019 |
|---|---|
| Recall event | 81562 |
| Product | ARJOHUNTLEIGH GETINGE GROUP Flites Passive Clip Sling - Product Usage: The Arjo Passive Clip Sling is a product intended for assisted transfer of patient/resident with limited ability to move. Designed to be used for one patient during hospital stay and assists the caregiver with everyday patient… |
| Product code | FSA |
| Recalling firm | ARJOHUNTLEIGH POLSKA Sp. z.o.o. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 19, 2021 |
| 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