Fresh Recalls

FDAClass I · Food · Recall H-1122-2026 · Recalled July 1, 2026

5# Sunflower Seeds C/NS recall — George J Howe Company, Inc.

Agency report date: July 1, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
5# Sunflower Seeds C/NS
Company / brand
George J Howe Company
Lot / serial / date codes
00501139
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,
Agency product description and boundaries

5# Sunflower Seeds C/NS

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class I: most serious — reasonable probability of serious health consequences or death.

Affected product: 5# Sunflower Seeds C/NS

3. Open the official notice or contact

Official recall ID
H-1122-2026
Brand
George J Howe Company
Classification
Class I
Units affected
7.00 Cases
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Grove City, PA, United States
Firm address
629 W Main St, N/A, 16127-1109

Identifying details (verbatim from the notice)

Product codes / lots
00501139
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,
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
98867
Recall initiated
April 29, 2026
FDA classified
June 24, 2026
FDA report date
July 1, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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