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CriticalFDAfda-F-0957-2023SALMONELLA CONTAMINATION

Living Nutz Nut & Seed Butter Raw Sprouted & Stoneground; 8 oz., 12 oz. or 64 oz.

⚠ Critical Alert — Stop Using Immediately

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

Category
Units Affected
68
Recall Date
May 11, 2023
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0957-2023.

Nut butter potentially contaminated by Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0957-2023.

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 Living Nutz Living Organic Foods 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-0957-2023.

Living Nutz Living Organic Foods

FDA

About the U.S. Food and Drug Administration

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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Living Nutz Living Organic Foods Recall FAQ

Living Nutz Living Organic Foods is the subject of a dairy safety report: Living Nutz Nut & Seed Butter Raw Sprouted & Stoneground; 8 oz., 12 oz. or 64 oz.. The notice was published on May 11, 2023 by the U.S. Food and Drug Administration (FDA). Approximately 68 units are potentially affected.