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RECALL RECORD — CLASS IIRecall completedF-2081-2016/FDA enforcement
Geneva Foods, LLC·Food·Feb 1, 2016

Lysander's All Natural Bourbon Flavor Rub

What you need to know

Class II

  • What happened

    Product contains undeclared allergens soy and wheat. Also does not declare sulfites.

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Fish-derived ingredients were omitted from the label, creating a risk for fish-allergic consumers.

  • Action required

    Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction.

Recall completed · classified by the FDANationwide (US)More food

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Product identification

Source: FDA FOOD

Brand nameGeneva Foods, LLC
Recalling firmGeneva Foods, LLCSanford, FL, United States
UPC / barcodes
0 34795 00049 5
Lot / date codes
  • Lot codes ending in 14 or 15
  • UPC: 0-34795-00049-5.
Distribution area
Nationwide

Distributed nationwide to the following states: AK, AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, MA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY.

United States

Quantity affected5, 145 cases (30, 870 units)
Recall initiationFDA report date: September 14, 2016
FDA recall numberF-2081-2016

Beyond the headline

The recall, in context

Geneva Foods, LLC initiated this food recall on February 1, 2016. The FDA enforcement report states: Product contains undeclared allergens soy and wheat. Also does not declare sulfites. The FDA report lists distribution as: Distributed nationwide to the following states: AK, AL, AZ, AR, CA, CO, CT, DE, FL, GA, ID, IL, IN, IA, KS, KY, LA, MA, MD, MA, MI, MN, MS, MO, MT, NE, NV, NH, NJ, NM, NY, NC, ND, OH, OR, PA, RI, SC, SD, TN, TX, UT, VT, VA, WA, WV, WI, WY.

The FDA enforcement report describes the reason as: Product contains undeclared allergens soy and wheat. Also does not declare sulfites.

Lysander's All Natural Bourbon Flavor Rub was made or distributed by Geneva Foods, LLC in Sanford, FL, United States. This page reflects FDA report F-2081-2016, dated September 14, 2016.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, an allergen that is present but missing or incorrect on the label can cause a serious reaction in allergic consumers.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Undeclared fish

Symptoms to watch for

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.

When symptoms may appear

Reactions can begin within minutes to a few hours after eating the product.

Higher-risk groups

People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.

What to do now

  1. 1Do not eat the product if you have a fish allergy.
  2. 2Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Lysander's All Natural Bourbon Flavor Rub recall?

Geneva Foods, LLC recalled Lysander's All Natural Bourbon Flavor Rub in an FDA Class II enforcement action reported as F-2081-2016. Product contains undeclared allergens soy and wheat. Also does not declare sulfites.

What are the symptoms of Undeclared fish exposure?

Hives, swelling, wheezing, vomiting or anaphylaxis can occur in people with a fish allergy.

How quickly can Undeclared fish symptoms appear?

Reactions can begin within minutes to a few hours after eating the product.

Who is most at risk from Undeclared fish?

People with a diagnosed fish allergy, especially anyone with a history of anaphylaxis.

What should I do if I bought this product?

Do not eat the product if you or someone in your household has a diagnosed allergy. Check the codes below, return it to the retailer for a refund, or dispose of it safely. Seek urgent care for signs of a severe allergic reaction. Do not eat the product if you have a fish allergy. Seek emergency care for breathing difficulty, throat swelling or other signs of anaphylaxis. Keep the packaging and contact the retailer or manufacturer about a refund.

How do I get a refund from Geneva Foods, LLC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall F-2081-2016 and keep the packaging, lot code and proof of purchase if you have them.

Is the Geneva Foods, LLC recall still active?

The FDA lists this recall as recall completed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-2081-2016. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.