Device recall
Z-0772-2007: Lumex Walkabout Lite Four-Wheel Rollator, Manufactured for: Graham-Field Health…
FDA device recall · Class II · Graham Field Atlanta
Key facts
| Recall number (Z-number) | Z-0772-2007 |
|---|---|
| Recall event | 37747 |
| Product | Lumex Walkabout Lite Four-Wheel Rollator, Manufactured for: Graham-Field Health Products, Atlanta, Georgia 30360. |
| Product code | ITJ |
| Recalling firm | Graham Field Atlanta |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2010 |
| FEI number | 2427360 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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