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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted December 26, 2024
Sleep Supplement Recalled Due to Undeclared Soy
On October 30, 2024, Deseret Biologicals Inc. recalled 2,547 bottles of DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules, which are labeled as containing phosphatidylserine from sunflower lecithin powder but contain undeclared soy lecithin.
People with an allergy to soy should not consume these products as they could cause a serious or life-threatening allergic reaction.
(See ConsumerLab’s Phosphatidylserine Supplements Review for tests of related products. Also see CL’s article about supplements to improve sleep).
Recalled DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules were distributed worldwide, with one foreign distributor to Australia. They can be further identified by the following:
- Product name: DesBio lunaSOMM Natural Sleep Support
- Packaging: Blue PET bottle with a white cap, containing 30 capsules
- Lot number: 020323126
Deseret Biologicals Inc is notifying consignees or the public of the recall by two or more of the following: email, fax, letter, press release, telephone, visit.
For more information, use the link below.
Enforcement Report: DesBio lunaSOMM Natural Sleep Support Dietary Supplement
See related recalls and warnings:
FDA Warns Seller of Melatonin & Other Sleep Supplements
Living Free Vitamins, Joint, Nerve and Other Supplements Recalled
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
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If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
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If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
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