Device recall
Z-3280-2011: Dual Blue-Release Adult Walkers - Wheeled, and Blue Release Junior Walkers with…
FDA device recall · Class II · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-3280-2011 |
|---|---|
| Recall event | 58556 |
| Product | Dual Blue-Release Adult Walkers - Wheeled, and Blue Release Junior Walkers with 5 inch Fixed Wheels, Model Numbers: 6240-5F and 6240-JR5F. The recalled product is packaged four (4) units per shipping box. Product Usage: The walkers are intended for people who need additional support to maintain… |
| Product code | ITJ |
| Recalling firm | Invacare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 2, 2013 |
| FEI number | 1525712 |
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