Z-2475-2020 Class II Terminated
FDA device recall Z-2475-2020 was initiated by Mueller Sports Medicine, Inc on June 18, 2020 and is designated Class II. Reason for recall: Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex". The recall status is terminated (terminated October 29, 2021). Affected quantity: 135,354 units.
Recall Details
- Product Type
- Devices
- Report Date
- July 8, 2020
- Initiation Date
- June 18, 2020
- Termination Date
- October 29, 2021
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 135,354 units
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".
Distribution Pattern
U.S. distribution only: AR and OH.
Code Information
Reference number: 64217, UPC number: 074676642178