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High RiskFDAfda-F-0731-2019UNDECLARED ALLERGEN

TURKEY HILL Vanilla Bean Premium Ice Cream #501 3 GAL (11.36L) paper carton CONTAINS: MILK Distributed By: Turkey Hill Dairy 2601 River R...

Category
Units Affected
866
Recall Date
November 15, 2018
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0731-2019.

Package did not contain Vanilla Bean Ice Cream but Cotton Candy Ice Cream, which contains soy lecithin that is not listed on the Vanilla Bean label.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0731-2019.

Recall ongoing. Follow firm instructions.

✅ 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 Harris Teeter Supermarkets, Llc Dba Hunter 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-0731-2019.

Harris Teeter Supermarkets, LLC dba Hunter 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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Harris Teeter Supermarkets, Llc Dba Hunter Farms Recall FAQ

Harris Teeter Supermarkets, Llc Dba Hunter Farms is the subject of a dairy safety report: TURKEY HILL Vanilla Bean Premium Ice Cream #501 3 GAL (11.36L) paper carton CONTAINS: MILK Distributed By: Turkey Hill Dairy 2601 River R.... The notice was published on November 15, 2018 by the U.S. Food and Drug Administration (FDA). Approximately 866 units are potentially affected.