25# Sunflower Seeds C/S Recalled for Undeclared Cashew Allergen
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George J Howe Company, Inc. is recalling 25# Sunflower Seeds C/S due to undeclared tree nut allergen (cashew). The Class I recall affects 2 cases distributed across multiple states.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 4, 2026 and geographically references United States. Its severity classification of "high" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Food.
What Happened
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Which Products Are Affected
25# Sunflower Seeds C/S (code info: 00601138), 2.00 Cases. 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. Recall number: H-1123-2026. Recalling firm: George J Howe Company, Inc., Grove City, PA.
What You Should Do
Consumers with a cashew allergy should not consume the product. Contact the recalling firm for further information on returns.
Why This Matters
Undeclared allergens in food products can cause serious or life-threatening allergic reactions in sensitive individuals.
Source
FDA recall H-1123-2026, Event ID 98867 (fda.gov)
Original source: FDA Official Notice ↗
Related FDA Recalls
All FDA Recalls →Nationwide notices with similar length or severity timing 8
Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (795 characters here).
Similar severity timing
Same severity (high) notices issued closest in time to August 4, 2026.
Frequently Asked Questions
Common questions about this FDA recall.