Recall map → All 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 StatesThis 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
View this record at the agency source →
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.