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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 100% Apple Juice Recalled for Potential Glass Chips

Agency Publication Date: July 3, 2023
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Summary

S. Martinelli Harvest Facility is recalling 2,387 cases (approximately 57,288 units) of Martinelli's Gold Medal 100% Apple Juice due to a potential glass quality issue. The recall affects 10 oz. apple-shaped glass bottles that may contain glass chips within the product. No injuries or incidents have been reported to date regarding this issue.

Risk

Ingesting glass chips can cause serious internal injuries, including cuts or lacerations to the mouth, throat, or digestive tract, and may also pose a choking hazard.

What You Should Do

  1. The recalled products are 10 oz. apple-shaped glass bottles of Martinelli's Gold Medal 100% Apple Juice with UPC code 041244000098 and production dates of May 4, 2023, or May 5, 2023.
  2. Check the pallet and batch numbers on your product 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 full refund, throw it away, or contact S. Martinelli Harvest Facility for further instructions.
  4. 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: Martinelli's Gold Medal 100% Apple Juice (10 oz)
Variants: Apple shaped glass bottles, Shelf stable
UPC Codes:
041244000098
Lot Numbers:
0001100265 (Production Date 5/4/2023)
0001100276 (Production Date 5/4/2023)
0001100290 (Production Date 5/4/2023)
0001100294 (Production Date 5/4/2023)
0001100305 (Production Date 5/4/2023)
0001100357 (Production Date 5/4/2023)
0001100365 (Production Date 5/4/2023)
0001100372 (Production Date 5/4/2023)
0001100377 (Production Date 5/4/2023)
0001100406 (Production Date 5/4/2023)
0001101144 (Production Date 5/5/2023)
0001101148 (Production Date 5/5/2023)
0001101154 (Production Date 5/5/2023)
0001101160 (Production Date 5/5/2023)
0001101166 (Production Date 5/5/2023)
0001101168 (Production Date 5/5/2023)
0001101177 (Production Date 5/5/2023)
0001101182 (Production Date 5/5/2023)
0001101189 (Production Date 5/5/2023)
0001101198 (Production Date 5/5/2023)
0001101199 (Production Date 5/5/2023)
0001101207 (Production Date 5/5/2023)
0001101211 (Production Date 5/5/2023)
0001101212 (Production Date 5/5/2023)
0001101214 (Production Date 5/5/2023)
0001101234 (Production Date 5/5/2023)
0001101235 (Production Date 5/5/2023)
0001101236 (Production Date 5/5/2023)
0001101278 (Production Date 5/5/2023)
0001101332 (Production Date 5/5/2023)
0001101358 (Production Date 5/5/2023)
GTIN:
041244000098

Recall #: F-1017-2023. Product sold in 24-unit cases.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92526
Status: Resolved
Manufacturer: S. Martinelli Harvest Facility
Sold By: 3 customers in RI, NY, and CA
Manufactured In: United States
Units Affected: 2,387 Cases; 57,288 units.
Distributed To: Rhode Island, New York, California

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.