Device recall
Z-1948-2012: Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street…
FDA device recall · Class II · Arjo, Inc. dba ArjoHuntleigh
Key facts
| Recall number (Z-number) | Z-1948-2012 |
|---|---|
| Recall event | 62116 |
| Product | Chorus Mobile Patient Lifter; manufactured by Arjo Ltd., St. Catherine Street, Gloucester, GL1 2SL, England, U.K.; Models KKB5060-21US, KKB5062-21US and KKB5080-21US. The Chorus is designed to be used as a standing and raising aid, it is useful for short transfers from one sitting position to… |
| Product code | FSA |
| Recalling firm | Arjo, Inc. dba ArjoHuntleigh |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 13, 2018 |
| FEI number | 1419652 |
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