Skip to main content
High RiskFDAfda-F-2880-2017UNDECLARED ALLERGEN

Nelson's Dutch Farms; Chocolate Chip Cookie Dough; Half Gallon; Nelson's Ice Cream, Inc., Royersford, PA 19468. Nelson's Dutch Farms...

Category
Units Affected
525
Recall Date
May 3, 2017
Issuing Agency
Hazard
Undeclared Allergen

FDA Recall Notice

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2880-2017.

The firm is recalling Chocolate Chip Cookie Dough as product labels failed to declare the allergens; wheat and Soy (from soy lecithin) as ingredients.

Corrective Action (per FDA)

Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2880-2017.

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 Nelson's Creamery, Llc. 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-2880-2017.

Nelson's Creamery, LLC.

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.

Visit FDA.gov →

📣 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.

How to report to FDAFile a report at FDA

Nelson's Creamery, Llc. Recall FAQ

Nelson's Creamery, Llc. is the subject of a dairy safety report: Nelson's Dutch Farms; Chocolate Chip Cookie Dough; Half Gallon; Nelson's Ice Cream, Inc., Royersford, PA 19468. Nelson's Dutch Farms.... The notice was published on May 3, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 525 units are potentially affected.