Severity
Moderate
ModerateClass IITerminated
FDA Devices recall · Reported July 8, 2020
Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box
Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex".
Compiled from official public sources by the editorial team.
Verify with FDA Devices →
Mueller Sports Medicine, Inc recalled Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box - a moderate-severity action.
Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box was recalled by Mueller Sports Medicine, Inc in July 8, 2020. Reason: Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex".. Check the official notice for the remedy. Verify recall #Z-2475-2020 with the FDA Devices before acting.
The recall
Mueller Sports Medicine, Inc issued this moderate-severity FDA Devices recall-Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex"..
- Moderate
- severity level
- 135K units
- affected scope
- Class II
- classification
- July 8, 2020
- reported
Sourced from official FDA Devices enforcement records. Verify recall #Z-2475-2020 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Devices action (record #Z-2475-2020) was formally reported on July 8, 2020, with the manufacturer initiating the action on June 18, 2020. It is classified under Moderate severity (Class II), with a current status of Terminated. Mueller Sports Medicine, Inc is listed as the recalling firm, operating out of Prairie Du Sac, WI. Federal records list the affected scope as 135,354 units, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex". Distribution data in the federal record shows the product reached: U.S. distribution only: AR and OH.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Medical Devices recalls over time
Where this recall sits in its category - 40,422 medical devices recalls on record
Where this recall sits in the database
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
135,354 units
Related Recalls
6
0 from same agency
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".
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | Z-2475-2020 |
| Date reported | July 8, 2020 |
| Date initiated | June 18, 2020 |
| Recalling firm | Mueller Sports Medicine, Inc |
| Firm location | Prairie Du Sac, WI |
| Affected scope | 135,354 units |
| Distribution | U.S. distribution only: AR and OH. |
Profile values are sourced directly from the official FDA Devices enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (Z-2475-2020) and product description against the item you own. Search the archive
- Confirm the current status with FDA Devices before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Devices record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Mueller Sports Medicine Hybrid Wraparound Knee Support, Qty: 1 unit per box. Recalled by Mueller Sports Medicine, Inc. Units affected: 135,354 units.
Why was this product recalled? ▼
Natural rubber is present in Hybrid Wraparound Knee Support labeled as "Not made with Natural Rubber latex".
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on July 8, 2020. Severity: Moderate. Recall number: Z-2475-2020.
Where was the recalled product distributed? ▼
Distribution: U.S. distribution only: AR and OH..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (Z-2475-2020) against your product. Visit the official FDA Devices website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
Should I stop using a recalled medication or medical device? ▼
Do not stop using a recalled medication or device without consulting your healthcare provider first, as abruptly discontinuing treatment could pose its own health risks. Your doctor can advise on alternatives or whether the recall applies to your specific product lot. Check the recall number and lot information against your product packaging.
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What to do next
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Devices, reported July 8, 2020.
- Source: FDA - Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC - Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA - National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.