US Food Recall Atlas

A single recall record, as the agency published it.

Recall mapAll recalls → 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***. MedOp Health, Inc. · reported 2015-08-12

Terminated This recall has been closed out by the agency.

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.
Classification
Class III
Recall initiated
2015-04-30
Reported by the agency
2015-08-12
Closed out (terminated)
2018-08-23
Recalling firm
MedOp Health, Inc.
Oldsmar, FL
United States

This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.

Distribution (the agency's own words)
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.
States we parsed from that text
AL AZ CA CT FL GA KS MA MD MI NC NE NJ NY OH OK PA RI TN TX WA WI

The agency named these states. Parse method explicit_state_list, confidence high.

Food category
Dietary supplements Produce (fruit & vegetables)derived

Assigned by a reviewed keyword rulebook over the product description, not by the agency.

Recall type
Voluntary: Firm initiated
Recall number
F-2942-2015

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.