Recall Z-2475-2020— Mueller Sports Medicine, Inc
Class II · Terminated
Class II FDA medical device recall by Mueller Sports Medicine, Inc, initiated 2020-06-18, terminated 2021-10-29. FDA's recall record names no specific 510(k) clearance for this event. 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"..
- Recalling firm
- Mueller Sports Medicine, Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2020-06-18
- Terminated
- 2021-10-29
- Firm location
- Prairie Du Sac, WI, United States
Product description
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".
Data sourced from openFDA. This site is unofficial and independent of the FDA.