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High RiskFDAfda-F-0825-2020UNDECLARED ALLERGEN

PREMIUM SELECTIONS BANANA PUDDING ICE CREAM NATURALLY & ARTIFICIALLY FLAVORED 1.5 QUART (1.42 L) KEEP FROZEN CONTAINS: MILK, WHEAT, COCON...

Category
Units Affected
4,417
Recall Date
February 11, 2020
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0825-2020.

The firm was notified that the product contains undeclared soy.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-0825-2020.

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-0825-2020.

Harris Teeter Supermarkets, LLC dba Hunter Farms

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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Harris Teeter Supermarkets, Llc Dba Hunter Farms Recall FAQ

Harris Teeter Supermarkets, Llc Dba Hunter Farms is the subject of a dairy safety report: PREMIUM SELECTIONS BANANA PUDDING ICE CREAM NATURALLY & ARTIFICIALLY FLAVORED 1.5 QUART (1.42 L) KEEP FROZEN CONTAINS: MILK, WHEAT, COCON.... The notice was published on February 11, 2020 by the U.S. Food and Drug Administration (FDA). Approximately 4,417 units are potentially affected.