RecallHawk
Class II Recall

Vermont Village Unsweetened Apple Sauce (24oz)

Stonewall Kitchen, LLC

Summary

The FDA issued a Class II for Vermont Village Unsweetened Apple Sauce (24oz) by Stonewall Kitchen, LLC. Reason: Product contains elevated levels of patulin..

Details

Source

Food Recall

External ID

F-0793-2024

Action Date

2024-01-31

Status

Terminated

Category

food

Product Description

Vermont Village Unsweetened Apple Sauce (24oz)

Lot/Code Info: Expiration dates: 10JUL2025 and 3OCT2025

Quantity Affected: 9027 units

Reason for Recall

Product contains elevated levels of patulin.

Distribution

AZ, NH, CA, CT, PA, NY, VT, RI, IA, IL, MD, ME, DE, NM, MA, NJ, MI, OH, GA, IN, SC, WA

Type: Voluntary: Firm initiated

Recall Initiated: 2024-01-02

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 85 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-0793-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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