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CriticalFDAfda-F-0936-2019SALMONELLA CONTAMINATION

Dakota Specialty Milling Enhanced Flax Flour Blend, 42205, Net Wt 50 lbs. Ground Flax, Calcium Sulfate, inulin, VM 112 (vitamin mix flou...

⚠ 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
11,750
Recall Date
December 21, 2018
Issuing Agency
Hazard
Salmonella Contamination

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0936-2019.

An ingredient in the blended products has the potential to be contaminated with Salmonella.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0936-2019.

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 Dakota Specialty Milling, Inc 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-0936-2019.

Dakota Specialty Milling, Inc

FDA

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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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Dakota Specialty Milling, Inc Recall FAQ

Dakota Specialty Milling, Inc is the subject of a supplements safety report: Dakota Specialty Milling Enhanced Flax Flour Blend, 42205, Net Wt 50 lbs. Ground Flax, Calcium Sulfate, inulin, VM 112 (vitamin mix flou.... The notice was published on December 21, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 11,750 units are potentially affected.