Class IIFood recall: undeclared soy
DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules
Deseret Biologicals Inc, of Sandy, UT, began recalling this product on . FDA classified the recall as Class II on .
Why it was recalled
In FDA’s words:
Product contains undeclared soy lecithin.
The allergen tags on this page are ours, matched from FDA’s words above.
The product
DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules
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.
- Codes and dates
- LOT 020323126 MFG 04/2023
- Quantity
- 2547 bottles
- Recall number
- F-0262-2025
Where it was distributed
In FDA’s words:
Distributed nationwide, one foreign distributor to Australia. No DOD distribution. No VA.
What Class II means
In FDA’s definitions, a Class II recall is one where: use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse health consequences is remote. FDA’s recall definitions
If you have this product
- FDA’s enforcement report doesn’t say what to do with a recalled product. FDA posts some companies’ recall announcements on its Recalls, Market Withdrawals and Safety Alerts page; not every recall has one.
- FDA doesn’t update a recall’s status after classifying it, so this page can’t tell you whether the recall is still open.
- If someone has a serious allergic reaction, call 911. Signs of a serious reaction
Source
FDA’s Enforcement Report, read through . This recall first appeared in the report of . openFDA asks that its data not be relied on for decisions about medical care. AllergyNest isn’t affiliated with or endorsed by FDA.