FDA recall record

Nutri-Force Nutrition Fish Oil Softgel Capsules in white High Density Poly-Ethylene recall — FDA F-1913-2014

Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as1000 mg Fish Oil soft gel…

Class IIclassification
F-1913-2014official record ID
May 7, 2014report date

Recall record at a glance

Official recordF-1913-2014
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNutri-Force Nutrition, Inc.
Report dateMay 7, 2014
Recall initiation dateApr 1, 2014
Quantity9,456
LocationMiami Lakes, FL, United States

Official product description

Fish Oil Softgel Capsules in white High Density Poly-Ethylene bottles labeled in part: "Major [brand] Fish Oil Cholesterol Free 1000 MG *** 100 Softgels *** Distributed by Major Pharmaceuticals ***Livonia, MI 48150 USA ***".

Why the product was recalled

Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as1000 mg Fish Oil soft gel capsules.

Distribution information

The entire lot was sold under two (2) sales orders with the final shipment taking place on 09/25/2013.

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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