Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC 362401 | 084648311285
Summary
The FDA issued a Class II for Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC 362401 | 08464831128 by Stonewall Kitchen, LLC. Reason: Product contains elevated levels of patulin.
Details
Source
Food Recall
External ID
F-0500-2024
Action Date
2023-12-13
Status
Terminated
Category
food
Product Description
Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC 362401 | 084648311285
Lot/Code Info: 31MAY2025
Quantity Affected: 13,086 units
Reason for Recall
Product contains elevated levels of patulin
Distribution
ME, AS, NH, CA, AR, NY, MA, VT, MD, NY, FL, MN, RI, IA, WA, MI, DE, NJ, OH, GA, IL, VA, PA, SC, CT, MN, SC, IN
Type: Voluntary: Firm initiated
Recall Initiated: 2023-11-17
Company
York, ME
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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Stonewall Kitchen, LLC has 4 FDA actions in our database, including 4 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 (Stonewall Kitchen, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Stonewall Kitchen, LLC have FDA actions?
Stonewall Kitchen, LLC has 4 FDA actions in our database, including 4 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0500-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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