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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/Beverages

Martinelli's Apple Juice Recalled for Potential Patulin Contamination

Agency Publication Date: April 22, 2025
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Summary

S Martinelli & Company is recalling approximately 7,234 cases of Martinelli's Apple Juice because it may contain elevated levels of patulin. The affected products are clear, bulbous glass bottles sold in 4-packs of 10-ounce bottles with a "Best By" date of December 5, 2026. Patulin is a naturally occurring toxin produced by mold that can sometimes develop in fruit juices.

Risk

Consumption of juice with high levels of patulin can cause nausea, vomiting, and digestive distress. No illnesses or injuries have been reported in connection with this recall to date.

What You Should Do

  1. This recall affects Martinelli's Apple Juice sold in 10-ounce bulbous glass bottles (4-pack) with UPC 041244641022 and a "Best By" date of 05DEC2026.
  2. Check the pallet or batch number printed on the packaging. See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a refund, throw it away, or contact S Martinelli & Company for further instructions.
  4. For additional questions, call the FDA Consumer Complaint hotline at 1-888-723-3332.

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: Martinelli's Apple Juice (10 oz)
Variants: 4-pack (6 packs per case), Bulbous/round glass bottle, White metal screw top lid
UPC Codes:
041244641022
Lot Numbers (120):
0001254859
0001255023
0001255026
0001254864
0001254917
0001254874
0001254984
0001254860
0001255030
0001255033
0001254901
0001254913
0001254884
0001254903
0001254857
0001255027
0001254861
0001254924
0001254957
0001254876
0001255001
0001254856
0001255020
0001254863
0001254909
0001254914
0001254873
0001254878
0001255009
0001254996
0001254987
0001254902
0001254972
0001254922
0001254872
0001255011
0001254993
0001254998
0001254921
0001254910
0001255015
0001254870
0001255028
0001254897
0001254983
0001254892
0001254919
0001254925
0001254887
0001255014
Date Ranges: BEST BY: 05DEC2026

Quantity: 7234 cases. Packaged as 4-10 oz bottles per pack with 6 packs per case.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 96542
Status: Resolved
Manufacturer: S Martinelli & Company
Sold By: Retail Stores
Manufactured In: United States
Units Affected: 7234 cases
Distributed To: Alabama, Arkansas, Arizona, California, Connecticut, Delaware, Florida, Georgia, Iowa, Illinois, Indiana, Kansas, Kentucky, Louisiana, Michigan, Missouri, Mississippi, North Carolina, New Hampshire, New Jersey, New York, Ohio, Pennsylvania, South Carolina, Texas, Utah, Virginia, Wisconsin
Agency Last Updated: May 16, 2025

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.