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FDA recall, , Moderate risk

Savannah Bee Company Honey BBQ Sauce Mustard

Honey BBQ Sauce Mustard may contain undeclared wheat and soy, posing a risk of serious allergic reaction.

Recall ended May 11, 2026. Still check yours.

What happened

Savannah Bee Company Inc. of Savannah, Georgia, recalled their HONEY BBQ SAUCE- MUSTARD, 16FL OZ bottles on February 27, 2026, after a customer notified the firm that the product was labeled as Mustard but contained a different flavor of BBQ sauce.

The investigation determined the product in the bottle is their Honey BBQ Sauce "Sweet," which contains wheat and soy that is not listed on the BBQ Sauce "Mustard" label. People who have an allergy or severe sensitivity to wheat or soy run the risk of serious or life-threatening allergic r.

The recalled product was shipped to 45 states including Alabama, Arkansas, Arizona, California, Florida, Georgia, New York, Texas, and Washington. The firm began the recall on February 27, 2026, and the FDA added it to the Enforcement Report on March 23, 2026.

2 photos

What to do

If a code on your package is listed below:

  1. Consumers who have purchased these products are urged to dispose of the product and request a full refund.
  2. Consumers with questions may contact customer service at 800-955-5080 M-F 8AM-5PM EST.
  3. All jars of honey with a “Honey BBQ Sauce-Mustard” Label with batch code B1L1360525 must be disposed of immediately as they may contain the “Honey BBQ Sauce-Sweet”.

Is yours affected?

Match the UPC and best-by date listed under your product.

A UPC is the number printed under a barcode.

  1. Honey BBQ Sauce Mustard

    UPC
    • 8 50033 93758 9
    Best-by date
    05/16/27

From the FDA notice

SAVANNAH BEE COMPANY HONEY BBQ SAUCE MUSTARD NET 16 FL OZ (453g), PACKED IN BOTTLES.

Recall details

Company began the recall
Company
Savannah Bee Company Inc.Savannah, Georgia
Risk

Moderate risk

Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.

FDA Class II recall · How risk is rated

Event ID
98500
Recall number
H-0615-2026
Quantity recalled
4,611/16 fl oz (453g) bottles

Timeline

FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.

  1. Company began the recall · Announced by the company

  2. Added to FDA's Enforcement Report · Classified by FDA

  3. In FDA's weekly enforcement report

  4. Listed on Recall Canary

  5. Recall ended

  6. Archived

  7. Summary updated

Summary by Recall Canary, written with AI · summary updated Oct 7, 2026 · primary source: U.S. Food and Drug Administration (opens in a new tab)