Product Wiki · Recalls · U.S. FDA — Food Enforcement

Recall F-2942-2015 — ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120 Vegetable Capsules***Distributed by MedOp, Inc., Oldsmar, FL 34677***www.medop.com***.

U.S. FDA — Food Enforcement · United States · 2015-04-30 · Class III

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Agency
U.S. FDA — Food Enforcement
Recall identifier
F-2942-2015
Date of alert
2015-04-30
Country / jurisdiction
United States
Risk level
Class III
Risk type
recall
Brand
MedOp Health, Inc.
Product category
food
Product type
Food
Barcode (EAN/GTIN)
32171215
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.