BarbaCuban Cubama White Truffle Sauce
Recalled by Prima Foods International, Inc.
Food recall
Prima Foods International, Inc.
Class III — least serious
Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
Prima Foods International, Inc. has recalled BarbaCuban Cubama White Truffle Sauce, according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on February 11, 2026 and was initiated on December 17, 2025. It is classified as a Class III recall, which means using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.
What was recalled?
This recall covers BarbaCuban Cubama White Truffle Sauce, with approximately 12,214 bottles total affected. The company behind the recall is Prima Foods International, Inc., based in Ocala, FL. The FDA describes the product as: “BarbaCuban Cubama White Truffle Sauce, Net Wt. 12 oz (355 ml). Packed in 12 oz glass bottles and 1 gallon HDPE Industrial Plastic Jugs, ¿ gallon HDPE Industrial Plastic Jugs. packaged in 12x12 fl oz, 6x12 fl oz, 4x1 gallon, 4x1/2 gallons. UPC code 7 19660 001…”
Why was BarbaCuban Cubama White Truffle Sauce recalled?
According to the FDA, the stated reason for the recall is: “Undeclared Quinine.” In plain terms, this recall relates to an undeclared ingredient or allergen.
An undeclared ingredient means a food contains something — often a major allergen such as milk, eggs, soy, wheat, peanuts, or tree nuts — that is not listed on the label. For most people this is not dangerous, but for someone with a food allergy or sensitivity it can trigger a serious reaction. Accurate labeling is required so that people can avoid ingredients they need to stay away from.
What should you do?
If you think you may have bought BarbaCuban Cubama White Truffle Sauce, compare it against the product description and identifying codes (Lot Codes: #233/24 Best by date: 02/2026) before using it.
The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact Prima Foods International, Inc. or your local health authority.
About this recall
This recall was distributed in FL. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.
Full recall details
- Status
- Terminated
- Date reported
- February 11, 2026
- Recall started
- December 17, 2025
- Distributed in
- FL
What you can do
Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.
Quick answers
Why was BarbaCuban Cubama White Truffle Sauce recalled?+
According to the FDA: Undeclared Quinine
How serious is this recall?+
Class III — least serious. Using this product is not likely to cause health problems, but it breaks an FDA rule (for example, a labeling or packaging issue).
What should I do if I have BarbaCuban Cubama White Truffle Sauce?+
Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.
Opens the U.S. Food and Drug Administration (FDA) data for this recall.
Recall number: H-0447-2026. Information last synced from the FDA on July 5, 2026.