MedOp Recalls MaxiFlex Multinutrient Formula Due to Out-of-Specification Raw Material
MedOp Health, Inc. is recalling MaxiFlex Multinutrient Formula dietary supplements because a material review found the Chondroitin Sulfate raw material used was out of specification.
The agency’s classification
FDA (Food): Class III
Class III is a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class III, which the rubric indicates is typically a score of 1 or 2. It is scored as 2 (Moderate) because it involves a raw material specification failure in a dietary supplement, which is a minor quality control issue rather than a cosmetic or documentation-only defect, but no illnesses are reported.
Plain-English summary
MedOp Health, Inc. is voluntarily recalling MaxiFlex (Registered) Multinutrient Formula, 120 Vegetable Capsules. The recall involves 638 bottles of the dietary supplement, distributed across 22 U.S. states including Alabama, Arizona, California, Connecticut, Florida, Georgia, Kansas, Massachusetts, Maryland, Michigan, Nebraska, North Carolina, New Jersey, New York, Ohio, Oklahoma, Pennsylvania, Rhode Island, Tennessee, Texas, Washington, and Wisconsin.
The recall was initiated after a material review conducted in April 2015 revealed that some of the Chondroitin Sulfate raw material (Lot 093011 1031) used in the manufacture of the product (Lot #32171215) was out of specification. The source text does not report any illnesses or injuries associated with this recall.
Consumers who purchased this product should check their lot numbers against the recall information. The source text does not provide specific instructions for consumers on how to dispose of or return the product, nor does it list a specific contact number for the recalling firm.
The recalled product
- Product
- ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120 Vegetable Capsules***Distributed by MedOp, Inc., Oldsmar, FL 34677***www.medop.com***.
- Manufacturer
- MedOp Health, Inc.
- Category
- Food — Dietary Supplement
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #32171215.
Distribution
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