Byron White FORMULAS A-FNG Herbal Supplement
Reason Label does not declare walnuts in English
Quantum Health branded Elderberry liquid herbal extract dietary supplement is packaged in recall
Recalled by Quantum Inc · Eugene, OR, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Product recalled due to potential contamination of 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
Quantum Health branded Elderberry liquid herbal extract dietary supplement is packaged in 2oz glass bottle, 12 bottles/case. Product is shelf stable with net wt. 2 fl oz/59 mL. UPC code: 0 46985 01625 4 Product is distributed by Quantum, Inc., Eugene, OR.
Quantity: 5 units
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.
Manufacturing code: "5831 09/23" Lot code is 5831 which is determined by order of production. It is not related to a date. Expiry is September 2023
Where it was sold
Indiana New Jersey New York
FDA's distribution note: Distributed in IN, NJ, and NY.
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
- Quantum Inc
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Nov 6, 2020
- In FDA report of
- Dec 9, 2020
- Terminated
- Jun 2, 2021
- FDA recall number
- F-0146-2021 · event 86726
- Official record
- FDA enforcement report search
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