Device recall
Z-2475-2020: Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box
FDA device recall · Class II · Mueller Sports Medicine, Inc
Key facts
| Recall number (Z-number) | Z-2475-2020 |
|---|---|
| Recall event | 85884 |
| Product | Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box |
| Product code | ITQ |
| Recalling firm | Mueller Sports Medicine, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2021 |
| FEI number | 2110420 |
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