Device recall
Z-0323-2009: Arjo Maxi 500 Patient Lift with 4 Point DPS (Dynamic Positioning System) and…
FDA device recall · Class II · Arjo, Inc.
Key facts
| Recall number (Z-number) | Z-0323-2009 |
|---|---|
| Recall event | 50079 |
| Product | Arjo Maxi 500 Patient Lift with 4 Point DPS (Dynamic Positioning System) and Scale; a Non-AC-Powered Patient Lift; Models KM560181; BHM Medical Inc., Magog, QC, Canada The Maxi 500 is a mobile passive lift intended to be for lifting and transferring of patients in hospitals, nursing homes, or other… |
| Product code | FSA |
| Recalling firm | Arjo, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 19, 2010 |
| 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