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.
Product description
***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120 Vegetable Capsules***Distributed by MedOp, Inc., Oldsmar, FL 34677***www.medop.com***.
Lot numbers, UPCs & expiration codes
Lot #32171215.
Where it was sold
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.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-2942-2015
- Classification
- Class III
- Status
- Terminated
- Recall initiated
- Apr 30, 2015
- FDA report date
- Aug 12, 2015
- Quantity
- 638 bottles (Containing 120 vegetable caps each)
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- MedOp Health, Inc.
Original FDA data
Every field from FDA enforcement report F-2942-2015, exactly as published.
Show all FDA fields
- City
- Oldsmar
- State
- FL
- Status
- Terminated
- Country
- United States
- Event ID
- 71145
- Address
- 630 Brooker Creek Blvd Ste 350
- Code information
- Lot #32171215.
- Postal code
- 34677-2928
- Report date
- Aug 12, 2015
- Product type
- Food
- Recall number
- F-2942-2015
- Classification
- Class III
- Recalling firm
- MedOp Health, Inc.
- Product quantity
- 638 bottles (Containing 120 vegetable caps each)
- Termination date
- Aug 23, 2018
- 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.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- ***MaxiFlex (Registered)***Multinutrient Formula***Maximum Joint Support***MedOp, Inc.***Dietary Supplement ***120 Vegetable Capsules***Distributed by MedOp, Inc., Oldsmar, FL 34677***www.medop.com***.
- Distribution pattern
- 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.
- Recall initiation date
- Apr 30, 2015
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Aug 6, 2015