Food Recall Check
Class II · Moderate risk Terminated Initiated Jun 12, 2023 (3 years ago)

Martinelli's Gold Medal 100% Apple Juice recall

Recalled by S. Martinelli Harvest Facility · Watsonville, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Potential glass quality issue that may result in glass chips in the product

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Martinelli's Gold Medal 100% Apple Juice 10 oz. glass bottles, 24 units per case Apple shaped glass bottles Shelf stable UPC: 041244000098

Quantity: 2,387 Cases; 57,288 units.

Food: Fresh fruit Juice & beverages

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Production Date 5/4/2023 Pallet/Batch 0001100265, 0001100276, 0001100290, 0001100294, 0001100305, 0001100357, 0001100365, 0001100372, 0001100377, 0001100406 Production Date 5/5/2023 Pallet/Batch 0001101144, 0001101148, 0001101154, 0001101160, 0001101166, 0001101168, 0001101177, 0001101182, 0001101189, 0001101198, 0001101199, 0001101207, 0001101211, 0001101212 0001101214, 0001101234, 0001101235, 0001101236, 0001101278, 0001101332, 0001101358

Where it was sold

California New York Rhode Island

FDA's distribution note: Product was shipped directly to 3 customers located in RI, NY, and CA

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
S. Martinelli Harvest Facility
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 12, 2023
In FDA report of
Jul 12, 2023
Terminated
Sep 3, 2024
FDA recall number
F-1017-2023 · event 92526
Official record
FDA enforcement report search

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