Device recall
Z-0479-2007: BHM Kwiktrak Fixed Gate component of the Kwiktrak rail system used with the Maxi…
FDA device recall · Class II · Arjo, Inc.
Key facts
| Recall number (Z-number) | Z-0479-2007 |
|---|---|
| Recall event | 36636 |
| Product | BHM Kwiktrak Fixed Gate component of the Kwiktrak rail system used with the Maxi Sky 600 Ceiling Patient Lift; Manufactured by BMH Medical Inc., 2001 Tanguay Street , Magog, Quebec, Canada J1X 5Y5. The fixed gate, part #700.11550, was sold in two kits: a) Part #700.11500 Kwiktrak Gate Kit composed… |
| Product code | FSA |
| Recalling firm | Arjo, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 9, 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