6/11oz No Salt Sunflower Seeds recall

Recalled by George J Howe Company, Inc. · Grove City, PA, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

Undeclared allergen: Tree nuts

For someone with a food allergy the label is the only protection. An undeclared allergen can trigger a severe reaction even in a trace amount, which is why most of these recalls are Class I. All undeclared allergens recalls.

What was recalled

6/11oz No Salt Sunflower Seeds

Quantity: 578.50 Cases

Food: Nuts & seeds

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

07317100320

Where it was sold

Alabama Arkansas Florida Georgia Iowa Illinois Indiana Kansas Kentucky Maryland Michigan Minnesota Missouri Mississippi North Carolina New Jersey New York Ohio Oklahoma Pennsylvania South Carolina Tennessee Virginia Wisconsin West Virginia

FDA's distribution note: The recalled product was distributed to the following States: AL, AR, FL, GA, IA, IL, IN, KS, KY, MD, MI, MN, MO, MS, NC, NJ, NY, OH, OK, PA, SC, TN, VA,WI,WV,

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. The risk from an undeclared allergen is to people allergic to tree nuts; for anyone else the product is generally not a safety concern. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm: George J Howe Company, Inc.
Initiated by: Voluntary: Firm initiated
Recall initiated: Apr 29, 2026
In FDA report of: Jul 1, 2026
Terminated: Sep 10, 2026
FDA recall number: H-1119-2026 · event 98867
Official record: FDA enforcement report search