Nelson's Dutch Farms; Death By Chocolate; Half Gallon; Nelson's Ice Cream, Inc., Royersford, PA 19468. Nelson's Dutch Farms; Death By...
⚠ Critical Alert — Stop Using Immediately
This product has been flagged with severe risks (serious injury or death). Stop using it now and contact the brand or FDA for a refund, repair, or replacement.
FDA Recall Notice
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2882-2017.
The firm is recalling Death By Chocolate ice cream products as product labels failed to declare the soy allergen (from soy lecithin) as ingredient.
Corrective Action (per FDA)
Source: U.S. Food and Drug Administration (FDA) — official FDA notice for recall FDA-F-2882-2017.
Recall terminated by FDA.
✅ What you should do
- Stop using the product if you own it.
- Check the model number, lot code, or sell-by date against the recall notice above.
- Contact Nelson's Creamery, Llc. or the retailer where you bought it for a refund, replacement, or repair.
- For the most current official instructions, visit the FDA recall page.
- 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-2882-2017.
Nelson's Creamery, LLC.
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.
Nelson's Creamery, Llc. Recall FAQ
Nelson's Creamery, Llc. is the subject of a dairy safety report: Nelson's Dutch Farms; Death By Chocolate; Half Gallon; Nelson's Ice Cream, Inc., Royersford, PA 19468. Nelson's Dutch Farms; Death By.... The notice was published on May 3, 2017 by the U.S. Food and Drug Administration (FDA). Approximately 548 units are potentially affected.