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CriticalFDAfda-F-0539-2021UNDECLARED ALLERGEN

Natural Way Almond Butter 16 oz. UPC 850001775175 packaged in clear plastic jars

⚠ Critical Alert — Stop Using Immediately

This product has been flagged with severe risks (undeclared allergen). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.

Category
Units Affected
2,166
Recall Date
May 4, 2021
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0539-2021.

Potential to contain undeclared peanuts

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0539-2021.

Recall terminated by FDA.

✅ What you should do

  1. Stop using the product if you own it.
  2. Check the model number, lot code, or sell-by date against the recall notice above.
  3. Contact Simkins Brothers Sweets, Llc Dba Natural Way Food Group or the retailer where you bought it for a refund, replacement, or repair.
  4. For the most current official instructions, visit the FDA recall page.
  5. If you've been hurt by this product, report the incident to FDA.

Consumer Contact (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0539-2021.

Simkins Brothers Sweets, LLC dba Natural Way Food Group

FDA

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The FDA regulates drugs, medical devices, food, cosmetics, and tobacco. Adverse event reports and recall notices are the main public safety signal.

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📣 Report a food, supplement, or cosmetic problem to the FDA

If you had a reaction, found contamination, or experienced a labeling problem with this product, report it to the FDA. The agency uses consumer reports to track emerging safety signals and trigger recalls.

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Simkins Brothers Sweets, Llc Dba Natural Way Food Group Recall FAQ

Simkins Brothers Sweets, Llc Dba Natural Way Food Group is the subject of a dairy safety report: Natural Way Almond Butter 16 oz. UPC 850001775175 packaged in clear plastic jars. The notice was published on May 4, 2021 by the U.S. Food and Drug Administration (FDA). Approximately 2,166 units are potentially affected.