# FDA recall Z-2475-2020

> **Mueller Sports Medicine, Inc** · Class II · device recall initiated 2020-06-18.

## 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".

## Distribution

U.S. distribution only: AR and OH.

## Key facts

- **Recall number:** Z-2475-2020
- **Recalling firm:** Mueller Sports Medicine, Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-06-18
- **Report date:** 2020-07-08
- **Termination date:** 2021-10-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Prairie Du Sac, WI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2475-2020

## Citation

> AI Analytics. FDA recall Z-2475-2020. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2475-2020. Source: US FDA. Licensed CC0.

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