pure solutions, inc.foodHigh PriorityActive

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)

pure solutions, inc. 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) was recalled by the FDA. Label declares bovine colostrum but does not declare milk allergen.

By RecallRadar Editorial Team

Sourced from FDA. Last reviewed March 4, 2026.

This recall involves safety concerns. Take action promptly.

Plain-English Summary

pure solutions, inc. 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) was recalled by the FDA. Label declares bovine colostrum but does not declare milk allergen.

Is This Recall Still Active?

Status: Yes - Active

This recall is currently active. If your device matches the affected models, follow the official instructions as soon as possible.

Source & Verification

This page summarizes the official notice and keeps key facts easy to verify.

Official source
FDA
Announced by source
February 3, 2026
Last reviewed by RecallRadar
March 4, 2026

What You Should Do

  1. 1## 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) Agency: FDA | Category: food | Date: 2026-02-03 Reason: Label declares bovine colostrum but does not declare milk allergen. What to do:
  2. 2Stop using the product if it matches your lot/model.
  3. 3Compare your product details with the FDA recall notice.
  4. 4Follow the manufacturer's remedy instructions (refund, replacement, or disposal).
Open Official Recall NoticeGet Alerts for pure solutions, inc. Devices

What's Being Recalled

Quoted source excerpt from the official notice.

Label declares bovine colostrum but does not declare milk allergen.

Who's Affected

Specific models and identifiers listed in the source notice:

Model #1

LOT: 0528D911 Expiration Date: May 2028

Technical model codes are manufacturer identifiers. Match both the product name and model code from your device settings, label, or packaging.

Frequently Asked Questions

Is my pure solutions, inc. device affected?

Check the affected models section on this page. The official notice currently lists LOT: 0528D911 Expiration Date: May 2028.

What is the remedy for this recall?

## 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) Agency: FDA | Category: food | Date: 2026-02-03 Reason: Label declares bovine colostrum but does not declare milk allergen. What to do: 1. Stop using the product if it matches your lot/model. 2. Compare your product details with the FDA recall notice. 3. Follow the manufacturer's remedy instructions (refund, replacement, or disposal).

Where can I verify recall details?

Use the official source link in this page to confirm dates, eligibility, and next steps: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Keep browsing with these internal hubs: pure solutions, inc. recall hub and Food & Drug recall hub.

Official Resources

Use these primary sources for final eligibility and claim instructions.

View official notice from FDA

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Quick Info

Brand
pure solutions, inc.
Category
food
Source Agency
FDA
Announced
February 3, 2026
Country
US
Status
Active

Source & Verification

Sourced from FDA. Last reviewed March 4, 2026.

Official source
FDA
Announced by source
February 3, 2026
Last reviewed by RecallRadar
March 4, 2026

Official Resources

Use these primary sources for final eligibility and claim instructions.

Open Official Recall NoticeView official notice from FDA

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