FDA Device recall Z-2475-2020
Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box
- FDA Device
- Class II
- terminated
- Published 2020-07-08
On 2020-07-08 the FDA classified a Class II recall of Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box by Mueller Sports Medicine, citing natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex".
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2475-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-06-18 |
| Published | 2020-07-08 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Mueller Sports Medicine |
| Distribution | AR, OH |
Product
Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box
Reason
Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex".
Identifiers
| upc | 074676642178 |
|---|---|
| code_info | Reference number: 64217, UPC number: 074676642178 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2475-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.