Mueller Sports Medicine Hybrid Wraparound Knee Support — Class II medical device recall Z-2475-2020
Terminated recall by Mueller Sports Medicine, Inc, reported 2020-07-08, distributed in AR, OH. Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex".
| Recall number | Z-2475-2020 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Mueller Sports Medicine, Inc, Prairie Du Sac, WI, United States |
| Recall initiated | 2020-06-18 |
| Classified | 2020-06-30 |
| Reported by FDA | 2020-07-08 |
| Terminated | 2021-10-29 |
| Distributed | AR, OH |
| Quantity | 135,354 units |
| Reason classes | labeling |
| UPC / GTIN / UDI-DI | 00074676642178 |
Product
Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box
Reason for recall
Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex".
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2475-2020. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.