Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
FIT&FOCUSED SUPPLEMENTS CLA 3000mg CONJUGATED LINOLEIC ACID LEAN BODY FORUMLA 135 SOFTGELS recall
Recalled by Fit and Focused Supplements · Canandaigua, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product may be contaminated with Salmonella.
Pathogen: Salmonella
Salmonella is the most common cause of food recalls for bacteria, often in eggs, produce, nuts and spices.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
FIT&FOCUSED SUPPLEMENTS CLA 3000mg CONJUGATED LINOLEIC ACID LEAN BODY FORUMLA 135 SOFTGELS; UPC: 7 28028 44036 2
Quantity: Approximately 420 units in storage with Amazon and 40 units to consumer
Food: Dietary supplements
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.
Batch Number: M11503
Where it was sold
Arizona California Colorado Florida Michigan Minnesota Missouri North Carolina North Dakota New Jersey New York Ohio Oregon Rhode Island Texas Utah Virginia
FDA's distribution note: MO, ND, FL, OR, NC, MI, FL, CO, NY, OH, AZ, UT, MN, CA, TX, RI, NJ, VA
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
- Fit and Focused Supplements
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 11, 2017
- In FDA report of
- Jul 26, 2017
- Terminated
- May 4, 2018
- FDA recall number
- F-2578-2017 · event 77536
- Official record
- FDA enforcement report search
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