RecallRadar
FDA · FoodClass I

Savor Seasonings LLC food recall: Organic Cheddar Type Seasoning

Undeclared allergens

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
99644
Recall initiated
Aug 7, 2026
Classified by FDA
Aug 28, 2026
Posted in Enforcement Report
Sep 9, 2026
Recalling firm
Savor Seasonings LLC
Firm location
Batavia, OH, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Product tested positive for undeclared milk allergen.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Aug 7, 2026. FDA classified it 21 days later, on Aug 28, 2026. Distribution reported by FDA: 1 consignee in Canada

Recalled products (1)

  • H-1319-2026 Class I Ongoing

    Organic Cheddar Type Seasoning, NET WT: 50 lbs. Product is packaged in bulk poly-lined paper bag. Savor Seasonings, LLC. 4292 Armstrong Boulevard Batavia, OH 45103. Product distribution: 218 (50-lb) bags + 2 partial bags (27-lb and 34-lb, one from each lot respectively).

    Codes / lots: Product Number: OCCHD00007-005 Lot: 11562, Batch: 1 and 2, Use By: 20270127 Lot: 11609, Batch: 1, 2, and 3, Use By: 20270211

    Quantity: 10,961 lbs

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 99644
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.