Device recall
Z-1637-2009: Flite Clip Slings; patient specific disposable sling; Manufactured in Belgium…
FDA device recall · Class II · ArjoHuntleigh
Key facts
| Recall number (Z-number) | Z-1637-2009 |
|---|---|
| Recall event | 51273 |
| Product | Flite Clip Slings; patient specific disposable sling; Manufactured in Belgium for Medibo NV, Heikant 5, 3930 Hamont Achel, Belgium; these slings are intended for use with Arjo and BHM Passive Patient Lifts and Ceiling Lifts with four-point hanger bars intended for use with clip slings. The slings… |
| Product code | FSA |
| Recalling firm | ArjoHuntleigh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 25, 2011 |
| FEI number | 3007515958 |
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