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FDA recall record

Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENERGY in all Body Cells***Dietary Supplement 30 SOFTGELS***."

Recall F-2951-2015Class IIITerminatedJuly 6, 2015

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of March 13, 2017. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENERGY in all Body Cells***Dietary Supplement 30 SOFTGELS***."

Reason

Product is mislabeled. Some of the Co Q 10 30 mg bottles were labeled with the incorrect label, Co Q 10 50 mg.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Coenzyme Q-10 50 mg label reads in part, "***Major***CO Q-10 50 MG***For healthy HEART & IMMUNE function***Promotes ENERGY in all Body Cells***Dietary Supplement 30 SOFTGELS***."

Code information listed by FDA

Product codes 700220/ 4211-30 Lot number 14378T, expiration date 08/2017.

Distribution and firm information

Recalling firm listed by FDA: Mason Vitamins, Inc.

Firm location listed by FDA: Miami Lakes, FL, United States

Distribution reported by FDA: OK, IL, FL, AZ, KS, OH, CA, AL, KY, TX, OR, MS, NJ, MA, WA, TN, MI, MN, UT, VA, NC, GA, PA, MO, NY, WI, NH, AK, CO, NE and Hawaii

Product quantity listed by FDA: 13,027 bottles (includes both labels)

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.