RecallHawk
Class II Recall

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

S. Martinelli Harvest Facility

Summary

The FDA issued a Class II for Martinelli's Gold Medal 100% Apple Juice 10 oz. glass bottles, 24 units per case by S. Martinelli Harvest Facility. Reason: Potential glass quality issue that may result in glass chips in the product.

Details

Source

Food Recall

External ID

F-1017-2023

Action Date

2023-07-12

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: 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

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

Reason for Recall

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

Distribution

Product was shipped directly to 3 customers located in RI, NY, and CA

Type: Voluntary: Firm initiated

Recall Initiated: 2023-06-12

Company

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 228 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (S. Martinelli Harvest Facility) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does S. Martinelli Harvest Facility have FDA actions?

This is the only FDA action we have on record for S. Martinelli Harvest Facility in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1017-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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