Device recall
Z-1557-2008: Medi-Lifter III Plus Total Lift, Model 7000-2000 and Summit Total Lift, Model…
FDA device recall · Class II · Arjo, Inc.
Key facts
| Recall number (Z-number) | Z-1557-2008 |
|---|---|
| Recall event | 47456 |
| Product | Medi-Lifter III Plus Total Lift, Model 7000-2000 and Summit Total Lift, Model 4800-2000; patient lifts with mast scale (600 lbs. capacity); Mast scale is Intended to be used for weighing patients while in the lifter. Manufactured by Medi-Man Rehabilitation Products Inc., 6200A Tomken Road… |
| Product code | FSA |
| Recalling firm | Arjo, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 18, 2009 |
| 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