Fit and Focused Supplements: Salmonella Risk in CLA Softgels
Fit and Focused Supplements recalls CLA 3000mg softgels due to possible Salmonella contamination. Consumers should check UPC 7 28028 44036 2 and batch M11503 for affected products.
Lower-risk recall
Product may be contaminated with Salmonella.
Contact the company
What happened, in plain English
Fit and Focused Supplements is recalling a specific CLA softgel formula due to potential Salmonella contamination. This could cause food poisoning if consumed, so affected consumers should stop using the product. Read more at govinfonow.com/recall/20883-fit-and-focused-supplements-salmonella-risk-in-cla-softgels.
Source Summary by GovInfoNow · govinfonow.com/recall/20883-fit-and-focused-supplements-salmonella-risk-in-cla-softgels · Updated October 8, 2026 · FDA enforcement record: FDA #F-2578-2017
Cite this page
“Fit and Focused Supplements: Salmonella Risk in CLA Softgels.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/20883-fit-and-focused-supplements-salmonella-risk-in-cla-softgels. Based on FDA recall #F-2578-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2578-2017%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning. If the softgels are contaminated, eating them could lead to stomach illness, fever, and diarrhea.
Who’s affected
Anyone who purchased the recalled softgels with UPC 7 28028 44036 2 and batch number M11503. People with weakened immune systems may be at higher risk from Salmonella.
How to tell if you have this one
Check for the UPC code 7 28028 44036 2 and batch number M11503 on the product label. The product is a CLA 3000mg conjugated linoleic acid softgel formula.
- Brand
Fit and Focused Supplements- Product
FIT&FOCUSED SUPPLEMENTS CLA 3000mg CONJUGATED LINOLEIC ACID LEAN BODY FORUMLA 135 SOFTGELS; UPC: 7 28028 44036 2- Category
Food
What to do — step by step
Check Product Label
Look for the UPC code 7 28028 44036 2 and batch number M11503 on the softgel container.
Where it went and when
Where it was distributed
Distributed in 17 states.
FDA distribution: “MO, ND, FL, OR, NC, MI, FL, CO, NY, OH, AZ, UT, MN, CA, TX, RI, NJ, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arizona, California, Colorado, Florida, Michigan, Minnesota, Missouri, New Jersey, New York, North Carolina, North Dakota, Ohio, Oregon, Rhode Island, Texas, Utah, Virginia.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-2578-2017 (June 11, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2578-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.