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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Food
Food & Beverages/Packaged & Processed

L & L Homemade Corn Salsa Recalled for Improper pH Levels

Agency Publication Date: December 6, 2024
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Summary

Levi A. Bontrager is recalling 192 jars of L & L Homemade Corn Salsa because the product has a pH level of 4.7, which is outside of safe production standards. This improper acidity level can lead to the growth of harmful bacteria. The salsa is sold in 16 oz glass jars and was distributed to retail locations in Illinois and Wisconsin. No incidents or illnesses have been reported to date.

Risk

Jarred foods with improper pH levels can support the growth of dangerous pathogens, including those that cause botulism, which can lead to serious food poisoning or death. The salsa had a pH of 4.7, which is above the safety threshold required to prevent bacterial growth in shelf-stable foods.

What You Should Do

  1. The recalled product is L & L Homemade Corn Salsa sold in 16 oz glass jars. Look for the 'Best By' date 'BB 4 17 26' printed on the top of the jar lids.
  2. Return the product to the place of purchase for a full refund, throw it away, or contact the manufacturer for further instructions.
  3. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA).

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: L & L Homemade Corn Salsa (16 oz)by L & L
Variants: 16 oz Glass jar
Lot Numbers:
BB 4 17 26

Manufacturer: Levi A. Bontrager, W1520 Starr Road, Granton, WI 54436; Recall #: F-0258-2025

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 95782
Status: Resolved
Manufacturer: Levi A. Bontrager
Sold By: Retailers in Illinois; Retailers in Wisconsin
Manufactured In: United States
Units Affected: 192 jars
Distributed To: Illinois, Wisconsin

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.