Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Fish Oil Softgel Capsules in white High Density Poly-Ethylene bottles labeled in part recall
Recalled by Nutri-Force Nutrition, Inc. · Miami Lakes, FL, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it 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.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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 ***".
Quantity: 9,456
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Lot #107945
Where it was sold
FDA's distribution note: The entire lot was sold under two (2) sales orders with the final shipment taking place on 09/25/2013.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Nutri-Force Nutrition, Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Apr 1, 2014
- In FDA report of
- May 7, 2014
- Terminated
- Sep 4, 2014
- FDA recall number
- F-1913-2014 · event 67999
- Official record
- FDA enforcement report search
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