Device recall
Z-1945-2009: Maxilift Patient Lift, Non-AC Powered; a patient lift with a four point tilting…
FDA device recall · Class II · ArjoHuntleigh
Key facts
| Recall number (Z-number) | Z-1945-2009 |
|---|---|
| Recall event | 52126 |
| Product | Maxilift Patient Lift, Non-AC Powered; a patient lift with a four point tilting frame, adjustable chassis, and optional electronic scale, to move patients in a hospital/nursing home situation; Arjo Inc., Roselle, IL 60172; Model numbers 21102406, 21200001, 21200006, 21000-01, 210024-06, 211010-06… |
| 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