Class II — Mueller Sports Medicine, Inc
| Recalling firm | MUELLER SPORTS MEDICINE, INC. |
|---|---|
| Registered facility | MUELLER SPORTS MEDICINE, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex". |
| Product | Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box |
| Quantity | 135,354 units |
| Distribution | U.S. distribution only: AR and OH. |
| Initiated | 2020-06-18 |
| Classified | 2020-06-30 |
| Terminated | 2021-10-29 |
| Recall number | Z-2475-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Mueller Sports Medicine, Inc (Z-2475-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85884/
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