Class IOngoingVoluntary: Firm initiated

Savor Seasonings LLC: food recall H-1319-2026

Savor Seasonings LLC of Batavia, OH recalled Organic Cheddar Type Seasoning, NET WT: 50 lbs. Product is packaged in bulk poly-lined paper bag. Savor Seasonings,… Reason: Product tested positive for undeclared milk allergen. The FDA listed it as Class I in its Enforcement Report dated Sep 9, 2026.

Record status as published: Ongoing. openFDA data last updated Oct 21, 2026.

Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.

Recall details

Product
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).
Product quantity
10,961 lbs
Reason for recall
Product tested positive for undeclared milk allergen.
Codes, lots and dates on the package
Product Number: OCCHD00007-005 Lot: 11562, Batch: 1 and 2, Use By: 20270127 Lot: 11609, Batch: 1, 2, and 3, Use By: 20270211
Distribution pattern
1 consignee in Canada
Recalling firm
Savor Seasonings LLC, Batavia, OH
Classification
Class I — the FDA uses this class for a situation in which there is a reasonable probability that using or being exposed to the product will cause serious adverse health consequences or death.
Voluntary or mandated
Voluntary: Firm initiated
How the firm first notified customers
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Dates

EventDate
Recall initiated by the firmAug 7, 2026
Classified by the FDAAug 28, 2026
Published in the Enforcement ReportSep 9, 2026

All food recall records

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Sources

  • U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-1319-2026 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
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