Device recall
Z-1949-2012: Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical…
FDA device recall · Class II · Arjo, Inc. dba ArjoHuntleigh
Key facts
| Recall number (Z-number) | Z-1949-2012 |
|---|---|
| Recall event | 62116 |
| Product | Sara Plus Mobile Patient Lifter; manufactured for Arjo by Medibo Medical Products N.V., Heikant 5, B-3930 Hamont-Achel, Belgium; Models HEP0001-US and HEP1001-US. The Sara Plus is a standing and raising aid for short transfers e.g. raising from bed and transfer to wheelchair, or from wheelchair 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