LowClass IIITerminated

FDA Food recall · Reported August 12, 2015

MaxiFlex (Registered)Multinutrient FormulaMaximum Joint SupportMedOp, Inc.Dietary Supplement 120 Vegetable CapsulesDistributed by MedOp, Inc., Oldsmar, FL 34677www.medop.com***.

Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable Capsules is being recalled because a material review was conducted in April 2015. It revealed some of the Ch…

Recall #: F-2942-2015
Affected scope: 638 bottles (Containing 120 vegetable caps each)
Initiated: April 30, 2015

Compiled from official public sources by the editorial team. · Updated August 2026

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MedOp Health, Inc. recalled ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***… - a low-severity action.

***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***… was recalled by MedOp Health, Inc. in August 12, 2015. Reason: Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable Capsules is being recalled because a ma…. Check the official notice for the remedy. Verify recall #F-2942-2015 with the FDA Food before acting.

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The recall

MedOp Health, Inc. issued this low-severity FDA Food recall-Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable Capsules is being recalled because a ma….

Low
severity level: Class III
classification: August 12, 2015
reported

Sourced from official FDA Food enforcement records. Verify recall #F-2942-2015 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.

Recall Insight

This FDA Food action (record #F-2942-2015) was formally reported on August 12, 2015, with the manufacturer initiating the action on April 30, 2015. It is classified under Low severity (Class III), with a current status of Terminated. MedOp Health, Inc. is listed as the recalling firm, operating out of Oldsmar, FL. Federal records list the affected scope as 638 bottles (Containing 120 vegetable caps each).

The documented reason for this recall is: Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable Capsules is being recalled because a material review was conducted in April 2015. It revealed some of the Chondroitin Sulfate (Lot 093011 1031) raw … Distribution data in the federal record shows the product reached: All US States: AL, AZ, CA, CT, FL, GA, KS, MA, MD, MI, NE, NC, NJ, NY, OH, OK, PA, RI, TN, TX, WA and WI.. 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, 2 from FDA Food - 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.

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 low severity.

Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.

Severity

Low

Affected scope

638 bottles (Containing 120 vegetable caps each)

Related Recalls

2 from same agency

Product description

Reason for recall

Maxivision MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable Capsules is being recalled because a material review was conducted in April 2015. It revealed some of the Chondroitin Sulfate (Lot 093011 1031) raw material used in the manufacture of Maxiflex Multinutrient Formula Lot 32171215 was Out of Specification.

Recall Profile

Structured summary of the FDA Food recall record
Attribute	Value
Agency	U.S. Food and Drug Administration
Severity class	Low (Class III)
Status	Terminated
Recall number	F-2942-2015
Date reported	August 12, 2015
Date initiated	April 30, 2015
Recalling firm	MedOp Health, Inc.
Firm location	Oldsmar, FL
Affected scope	638 bottles (Containing 120 vegetable caps each)
Distribution	All US States: AL, AZ, CA, CT, FL, GA, KS, MA, MD, MI, NE, NC, NJ, NY, OH, OK, PA, RI, TN, TX, WA and WI.

Profile values are sourced directly from the official FDA Food 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 (F-2942-2015) and product description against the item you own. Search the archive
Confirm the current status with FDA Food 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 Food 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? ▼

***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120 Vegetable Capsules***Distributed by MedOp, Inc., Oldsmar, FL 34677***www.medop.com***.. Recalled by MedOp Health, Inc.. Units affected: 638 bottles (Containing 120 vegetable caps each).

Why was this product recalled? ▼

Which agency issued this recall? ▼

This recall was issued by the FDA Food on August 12, 2015. Severity: Low. Recall number: F-2942-2015.

Where was the recalled product distributed? ▼

Distribution: All US States: AL, AZ, CA, CT, FL, GA, KS, MA, MD, MI, NE, NC, NJ, NY, OH, OK, PA, RI, TN, TX, WA and WI..

How do I check if my product is affected by a recall? ▼

Check the product description and recall number (F-2942-2015) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.

What are the health risks of consuming a recalled food product? ▼

Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.

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Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported August 12, 2015. 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.