MedOp recalls 120-veg capsule joint supplement due to chondroitin sulfate raw material out of specification. No remedy stated in recall notice.
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.
MedOp is recalling its MaxiFlex Maximum Joint Support dietary supplement because the chondroitin sulfate used in production was found out of specification. This could potentially affect product quality but the recall does not specify a safety hazard.
The recall states that chondroitin sulfate raw material (Lot 093011 1031) used in production was out of specification. This means the supplement may not meet quality standards, but the recall does not indicate a safety hazard.
Owners of the 120-veg capsule MaxiFlex Maximum Joint Support supplement (Lot 32171215) distributed by MedOp, Inc. in Oldsmar, FL. People using this supplement for joint health are most at risk.
Check for the product name 'MaxiFlex Maximum Joint Support' with 120 vegetable capsules. Look for the lot number 32171215 on the label. The product was distributed by MedOp, Inc. in Oldsmar, FL.
Verify the product name, lot number, and distribution details to confirm if it matches the recalled items.
The recall states the chondroitin sulfate raw material was out of specification, but does not indicate a safety hazard. The product is not considered dangerous.
The recall notice does not specify a remedy, so no action is required beyond checking if you have the recalled product.
Check for the product name 'MaxiFlex Maximum Joint Support' with 120 vegetable capsules and lot number 32171215.
We’ve drafted a message you can send MedOp to request your refund or repair — edit it as you like.
Subject: Recall F-2942-2015 — MedOp MedOp Hello, I own a MedOp that is covered by recall F-2942-2015 from MedOp. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
