Summary
The FDA issued a Class I for 5# Sunflower Seeds C/S by George J Howe Company, Inc.. Reason: The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew..
Details
Source
Food Recall
External ID
H-1121-2026
Action Date
2026-07-01
Status
Ongoing
Category
food
Product Description
5# Sunflower Seeds C/S
Lot/Code Info: 00501138
Quantity Affected: 19.00 Cases
Reason for Recall
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Distribution
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,
Type: Voluntary: Firm initiated
Recall Initiated: 2026-04-29
Company
Grove City, PA
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 58 food recalls issued in the same week, part of 101 food-related FDA actions this month.
George J Howe Company, Inc. has 6 FDA actions in our database, including 6 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (George J Howe Company, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does George J Howe Company, Inc. have FDA actions?
George J Howe Company, Inc. has 6 FDA actions in our database, including 6 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-1121-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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