Class IOngoing · reported 2026-07-01

5# Sunflower Seeds C/S

George J Howe Company, Inc. recalled this product and the FDA reported the enforcement action on 1 July 2026 as Class I. The recall was initiated by the firm. The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.

The record

Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.

Product
5# Sunflower Seeds C/S
Reason for recall
The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.
Firm location
Grove City, Pennsylvania, United States
Classification
Class I
Status
Ongoing
Recall number
H-1121-2026
Quantity
19.00 Cases
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,
Initiated
29 April 2026
Reported by FDA
1 July 2026
Firm notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product codes
00501138

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
  • The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
  • This is one of 6 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 6 separate recalls, which almost every published figure does, overstates it by a factor of 6. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 6 of them.
  • This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
  • The distribution pattern names 24 states, and the FDA published the enforcement report 2 months after the firm began the recall.
  • Nuts and seeds carry both hazards at once: they are a major allergen in their own right, and as a low-moisture food they hold Salmonella for months without supporting its growth, which is why a nut butter recall can trace to a lot pressed a year earlier.

Named in the distribution pattern: 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. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.

What this recall was for

Undeclared allergens

An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.

A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.

21 CFR 117.135(c)(2)
Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
21 CFR 101.4
Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
21 CFR 117 subpart G
Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.

The allergens named in this record: tree nuts.

Filed under nuts and seeds. A product can sit in more than one.

Other nuts and seeds recalls for the same reason

These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.

ReportedProductFirmReasonClass
2026-09-02Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053KHONG GUAN (HQ)Undeclared peanuts.Class I
2026-09-02Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404Byron White Formulas, Inc.Label does not declare walnuts in EnglishClass II
2026-09-02BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000084KHONG GUAN (HQ)Undeclared peanuts.Class I
2026-09-02Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404Byron White Formulas, Inc.Label does not declare walnuts in EnglishClass II
2026-09-02Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404Byron White Formulas, Inc.Label does not declare walnuts in EnglishClass II
2026-08-19Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.Bazzini LLCUndeclared peanutsClass I
2026-07-22Ice Pop, D'Dioses Pistachio, 1 Bar (81.7 g), with UPC 827912008487D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-08FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, MILK FAT, SOY LECITHIN - AN EMULSIFIER, NATURAL VANILLA FLAVOR), RAISINS, TAPIOCA DEXTRIN, CONFECTIONERS GLAZE. CONTAINS: MILK, SOY PACKED IN A FAICLITY THAT HANDLES PEANUTS, TREE NUTS, WHEAT, SOY, EGG, SESAME, AND MILK PRODUCTS.Western Mixers Produce & Nuts, Inc.Undeclared peanuts.Class I

Other records from George J Howe Company, Inc.

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 5 other records name this firm.

ReportedProductFirmReasonClass
2026-07-016/11oz No Salt Sunflower SeedsGeorge J Howe Company, Inc.The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.Class I
2026-07-0125# Sunflower Seeds C/SGeorge J Howe Company, Inc.The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.Class I
2026-07-018/9.5oz Tub Nut - Sunflower SeedGeorge J Howe Company, Inc.The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.Class I
2026-07-015# Sunflower Seeds C/NSGeorge J Howe Company, Inc.The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.Class I
2026-07-016/11oz Sunflower Seeds SaltedGeorge J Howe Company, Inc.The firm is recalling sunflower seed products due to the presence of an undeclared tree nut allergen, cashew.Class I

All 6 records for George J Howe Company, Inc.

All 2026 recalls · All FDA food recall data

21 CFR 117.135(c)(2) is the clause behind this recall, and it is one somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.

Early access

Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.