Home / Recalls / Mueller Sports Medicine, Inc / Z-2475-2020

Z-2475-2020 Class II Terminated

Recalled by Mueller Sports Medicine, Inc — Prairie Du Sac, WI

FDA device recall Z-2475-2020 was initiated by Mueller Sports Medicine, Inc on Jun 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 Oct 29, 2021). Affected quantity: 135,354 units.

Recall details

Product Type: Devices
Report Date: Jul 8, 2020
Initiation Date: Jun 18, 2020
Termination Date: Oct 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

Source

Dataset: openFDA device recall enforcement reports
FDA record: This recall in openFDA (JSON)
Enforcement Report: Search FDA's Enforcement Report for Z-2475-2020
openFDA file date: Nov 10, 2026
Loaded by RegDataLab: Nov 11, 2026

These dates say when openFDA published the data file and when RegDataLab last loaded it.