Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp recall
Recalled by MedOp Health, Inc. · Oldsmar, FL, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
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.
See the recall's own reason text for the specifics. All other reasons recalls.
What 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***.
Quantity: 638 bottles (Containing 120 vegetable caps each)
Food: Dietary supplements
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot #32171215.
Where it was sold
Alabama Arizona California Connecticut Florida Georgia Kansas Massachusetts Maryland Michigan North Carolina Nebraska New Jersey New York Ohio Oklahoma Pennsylvania Rhode Island Tennessee Texas Washington Wisconsin
FDA's distribution note: 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.
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- MedOp Health, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 30, 2015
- In FDA report of
- Aug 12, 2015
- Terminated
- Aug 23, 2018
- FDA recall number
- F-2942-2015 · event 71145
- Official record
- FDA enforcement report search
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