Why it was recalled
Label declares bovine colostrum but does not declare milk allergen.
Product description
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)
Lot numbers, UPCs & expiration codes
LOT: 0528D911 Expiration Date: May 2028
Where it was sold
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 if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- H-0537-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Feb 3, 2026
- FDA report date
- Feb 25, 2026
- Quantity
- 442 units (bottles)
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Pure Solutions, Inc.
Original FDA data
Every field from FDA enforcement report H-0537-2026, exactly as published.
Show all FDA fields
- City
- Tampa
- State
- FL
- Status
- Ongoing
- Country
- United States
- Event ID
- 98413
- Address
- 14100 Mccormick Dr
- Code information
- LOT: 0528D911 Expiration Date: May 2028
- Postal code
- 33626-3018
- Report date
- Feb 25, 2026
- Product type
- Food
- Recall number
- H-0537-2026
- Classification
- Class II
- Recalling firm
- Pure Solutions, Inc.
- Product quantity
- 442 units (bottles)
- Reason for recall
- Label declares bovine colostrum but does not declare milk allergen.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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 pattern
- 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
- Recall initiation date
- Feb 3, 2026
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Center classification date
- Feb 27, 2026