Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported May 7, 2014
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 ***".
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.
The recall
Nutri-Force Nutrition, Inc. issued this moderate-severity FDA Food recall — Conjugated Linoleic Acid (CLA) softgel capsules and Fish Oil capsules were found mixed together in a retail b….
- Moderate
- severity level
- 9K units
- affected scope
- Class II
- classification
- May 7, 2014
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1913-2014 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1913-2014) was formally reported on May 7, 2014, with the manufacturer initiating the action on April 1, 2014. It is classified under Moderate severity (Class II), with a current status of Terminated. Nutri-Force Nutrition, Inc. is listed as the recalling firm, operating out of Miami Lakes, FL. Federal records list the affected scope as 9,456.
The documented reason for this recall is: 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 data in the federal record shows the product reached: The entire lot was sold under two (2) sales orders with the final shipment taking place on 09/25/2013.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food — clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Food recalls over time
Where this recall sits in its category — 22,938 food recalls on record
Where this recall sits in the database
Of 83,949 recalls in the database, 21,198 are high severity, 58,883 moderate, and 3,868 low. This recall is classified moderate severity.
Affected scope
9,456
Related Recalls
6
6 from same agency
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 ***".
Reason for recall
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.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1913-2014 |
| Date reported | May 7, 2014 |
| Date initiated | April 1, 2014 |
| Recalling firm | Nutri-Force Nutrition, Inc. |
| Firm location | Miami Lakes, FL |
| Affected scope | 9,456 |
| Distribution | The entire lot was sold under two (2) sales orders with the final shipment taking place on 09/25/2013. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
Frequently Asked Questions
What product 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 ***".. Recalled by Nutri-Force Nutrition, Inc.. Units affected: 9,456.
Why was this product 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.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on May 7, 2014. Severity: Moderate. Recall number: F-1913-2014.
Where was the recalled product distributed? ▼
Distribution: The entire lot was sold under two (2) sales orders with the final shipment taking place on 09/25/2013..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1913-2014) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
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Data Sources
Source: FDA, CPSC, and NHTSA federal recall databases. This recall: FDA Food, reported May 7, 2014.
- Source: FDA — Food and Drug Administration, openFDA Enforcement API (food, drug, and medical device recalls)
- Source: CPSC — Consumer Product Safety Commission Recalls API (consumer product recalls and hazards)
- Source: NHTSA — National Highway Traffic Safety Administration Recalls API (vehicle safety recalls)
Recall information is sourced from official federal agency databases. Always verify recall details with the issuing agency for the most current status. This information is for research and awareness purposes only.
Read our methodology — how this data is sourced, computed, and verified.
Source: Federal recall agencies (FDA, CPSC, NHTSA) Aggregated federal recall feeds Recall data normalized across FDA, CPSC and NHTSA feeds; severity classifications follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type).