FDA recall record

World Organic Theravits 100, container sizes: 30, 60, 90, 180, Product Code recall — FDA F-1544-2017

World Organic Corporation dba Licata Enterprise is recalling multiple vitamins because it contains fish liver oil that is declared on the product label;…

Class IIclassification
F-1544-2017official record ID
Mar 8, 2017report date

Recall record at a glance

Official recordF-1544-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmWorld Organic Corp.
Report dateMar 8, 2017
Recall initiation dateFeb 13, 2017
Quantity54,262 tablets total
LocationHuntington Beach, CA, United States

Official product description

Theravits 100, container sizes: 30, 60, 90, 180, Product Code: 0783-30, 0786-60, 0789-90, 0788-180; The Supreme One, Container sizes: 30,60,90,180, Product Code: 680-030, 680-060, 680-090, 680-180. The Supreme One and Theravits 100 product is sold under the brand names of Natures Concept, VP Discount, Clarks Nutrition, Hsu & Co, Spatz, Weber Health Foods, Harvest Natural Foods, Natures Nutrition, Vita Sun, Good Health, Kraskis, Lynden Nutrition, Seaside Health Foods, and Vita-Vista.

Why the product was recalled

World Organic Corporation dba Licata Enterprise is recalling multiple vitamins because it contains fish liver oil that is declared on the product label; however, the label also states "Contains NO...common allergens." The product also contains the following dietary ingredients that are missing from the label: molybdenum, pancreatin, diastase, papain, ox bile, vanadium, silicon, boron and bromelain.

Distribution information

US: WY, TX, VA, UT, ID, WA, OR, CA, OH, PA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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