Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 30, 2024 (2 years ago)

DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules recall

Recalled by Deseret Biologicals Inc · Sandy, UT, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product contains undeclared soy lecithin.

Undeclared allergen: Soy

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, 30 count in a Blue PET bottle with a White cap. Supplement facts declare Phosphatidylserine (from non-GMO sunflower lecithin powder) 40 mg. Distributed by Deseret Biologicals Inc 469 West Parkland Dr, Sandy, UT.

Quantity: 2547 bottles

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.

LOT 020323126 MFG 04/2023

Where it was sold

Nationwide.

Virginia

FDA's distribution note: Distributed nationwide, one foreign distributor to Australia. No DOD distribution. No VA.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. The risk from an undeclared allergen is to people allergic to soy; for anyone else the product is generally not a safety concern. 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
Deseret Biologicals Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 30, 2024
In FDA report of
Dec 18, 2024
Terminated
Sep 24, 2025
FDA recall number
F-0262-2025 · event 95737
Official record
FDA enforcement report search

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