Fish Oil Softgels Recalled Due to Mixed Conjugated Linoleic Acid Capsules
Nutri-Force Nutrition is recalling Fish Oil Softgel Capsules because Conjugated Linoleic Acid capsules were found mixed in the bottles.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, and the source text does not report any illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Nutri-Force Nutrition, Inc. is recalling 9,456 bottles of Fish Oil Softgel Capsules. The product is distributed by Major Pharmaceuticals and labeled as 1000 mg Fish Oil soft gel capsules.
The recall was initiated because Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail bottle labeled as 1000 mg Fish Oil soft gel capsules. The entire lot was sold under two sales orders, with the final shipment taking place on September 25, 2013.
Consumers who have purchased this product should stop using it and return it to the place of purchase or contact the recalling firm for instructions.
The recalled product
- Product
- 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 ***".
- Manufacturer
- Nutri-Force Nutrition, Inc.
- Category
- Food — Dietary Supplements
- Affected units
- 9,456
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot #107945
Distribution
Distribution scope not specified by the agency.
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