Martinelli's Gold Medal Apple Juice 1 liter (33.8 oz.) glass bottle UPC: 4124400102 6 Bottles per bundled shrink-wrapped
Summary
The FDA issued a Class II for Martinelli's Gold Medal Apple Juice 1 liter (33.8 oz.) glass bottle UPC: 4124400 by S Martinelli & Company. Reason: Product test results found the product to have elevated Patulin levels.
Details
Source
Food Recall
External ID
F-0254-2023
Action Date
2023-01-18
Status
Terminated
Category
food
Product Description
Martinelli's Gold Medal Apple Juice 1 liter (33.8 oz.) glass bottle UPC: 4124400102 6 Bottles per bundled shrink-wrapped pack/case.
Lot/Code Info: BEST BY 11AUG2025
Quantity Affected: 3,280 case (19,680 units)
Reason for Recall
Product test results found the product to have elevated Patulin levels
Distribution
US Only- CA, TX, NY, WA, UT, GA, OR, AZ
Type: Voluntary: Firm initiated
Recall Initiated: 2022-12-29
Company
Watsonville, CA
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 49 food recalls issued in the same week, part of 204 food-related FDA actions this month.
S Martinelli & Company has 3 FDA actions in our database, including 3 recalls.
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 & Company) 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 & Company have FDA actions?
S Martinelli & Company has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0254-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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