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CriticalFDAfda-F-0384-2018UNDECLARED ALLERGEN

Lunds & Byrels Dark Chocolate Almond 12/11oz.

⚠ 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.

Units Affected
201
Recall Date
October 31, 2017
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0384-2018.

The firms supplier has notified them that milk fat was missing from the ingredient statement and that the product label was missing the contains milk statement.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0384-2018.

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 United Natural Trading Inc. Dba Woodstock Farms 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-0384-2018.

United Natural Trading Inc. dba Woodstock Farms

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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United Natural Trading Inc. Dba Woodstock Farms Recall FAQ

United Natural Trading Inc. Dba Woodstock Farms is the subject of a snacks & candy safety report: Lunds & Byrels Dark Chocolate Almond 12/11oz.. The notice was published on October 31, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 201 units are potentially affected.