Pure Solutions, Inc. recalls Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset

Pure Solutions, Inc. started this recall on February 3, 2026. The FDA classified it as Class II, a middle category: eating the product may cause temporary or medically reversible health problems, and serious harm is unlikely. The reason given is undeclared allergen. It was distributed in 36 states. This recall is no longer considered active, but recalled products can stay in pantries and freezers for months.

Status: Closed / older
Recall started: February 3, 2026
Company: Pure Solutions, Inc.
Classification: Class II (temporary or reversible health risk)
Where sold: Arkansas, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Michigan, Minnesota, Missouri, North Carolina, North Dakota, Nebraska, New Jersey, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia, Wyoming
Quantity: 442 units (bottles)

Reason for recall (official wording)

Label declares bovine colostrum but does not declare milk allergen.

Recalled product (official wording)

Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep Reset, Net Wt., 1 fl oz (30 ml) liquid dietary supplement, Glass bottle with dropper cap. (Individual 1 fl oz bottles (not sold in case lots)

Distribution

Product was distributed to: AR, FL, CO, CA, CT, HI, IN, IL, ID, IA, KS, KY, LA, OH, OK, OR, MA, MI, MN, MO, GA, NC, NE, ND, NY, PA, SC, TN, NJ, UT, TX, VA , WA, WV, WI, WY

What to do

Compare the brand, size, lot code and dates on your package with the details above. If they match, do not eat it. Throw it away or return it to the store. Contact a healthcare provider if you feel unwell. Step-by-step guide.

Source: FDA Enforcement Report (openFDA), event 98413.