CLASS I Food recall · Reported 26 Jul 2017 · FDA Enforcement Report
Cla 3000mg Conjugated Linoleic Acid Lean Body Forumla recalled
Fit and Focused Supplements is recalling Fit&focused Supplements Cla 3000mg Conjugated Linoleic Acid Lean Body Forumla, distributed in 17 states. The recall was initiated on 11 Jun 2017 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- F-2578-2017
- FDA event ID
- 77536
- Recalling firm
- Fit and Focused Supplements, Canandaigua, NY
- Brand
- Fit&focused
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 11 Jun 2017
- FDA classified
- 14 Jul 2017
- Reported
- 26 Jul 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Salmonella
- Product category
- Dietary Supplements
Timeline
| 11 Jun 2017 | Recall initiated by company | |
| 14 Jul 2017 | Classified by FDA | +33 days |
| 26 Jul 2017 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Product may be contaminated with Salmonella.
Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.
Product as listed by the FDA
FIT&FOCUSED SUPPLEMENTS CLA 3000mg CONJUGATED LINOLEIC ACID LEAN BODY FORUMLA 135 SOFTGELS; UPC: 7 28028 44036 2
Where it was distributed
MO, ND, FL, OR, NC, MI, FL, CO, NY, OH, AZ, UT, MN, CA, TX, RI, NJ, VA
ArizonaCaliforniaColoradoFloridaMichiganMinnesotaMissouriNorth CarolinaNorth DakotaNew JerseyNew YorkOhioOregonRhode IslandTexasUtahVirginia
Questions about this recall
Is Cla 3000mg Conjugated Linoleic Acid Lean Body Forumla recalled?
Yes. Fit and Focused Supplements recalled Cla 3000mg Conjugated Linoleic Acid Lean Body Forumla on 11 Jun 2017. The recall is Class I and its status is Terminated. Recall number F-2578-2017.
Why was it recalled?
Product may be contaminated with Salmonella.
Which lots are affected?
Batch Number: M11503
Where was it sold?
MO, ND, FL, OR, NC, MI, FL, CO, NY, OH, AZ, UT, MN, CA, TX, RI, NJ, VA
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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