Device recall
Z-1046-04: Alenti Lift Hygiene Chair; a non-AC-powered patient lift; Arjo, Inc., 50 N. Gary…
FDA device recall · Class I · Arjo, Inc.
Key facts
| Recall number (Z-number) | Z-1046-04 |
|---|---|
| Recall event | 29137 |
| Product | Alenti Lift Hygiene Chair; a non-AC-powered patient lift; Arjo, Inc., 50 N. Gary Ave., Roselle, IL 60172; model numbers CDB8003-01-US and CDB8053-01-US (with scale) |
| Product code | FSA |
| Recalling firm | Arjo, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 13, 2004 |
| 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