My Wife's Slaw Jalapeno Heat, packaged in 8 oz. and 16 oz. glass mason jars with metal lids/bands, MyWifeslaw.web.app, Z
Summary
The FDA issued a Class II for My Wife's Slaw Jalapeno Heat, packaged in 8 oz. and 16 oz. glass mason jars with by Jesse Withrow. Reason: Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameter.
Details
Source
Food Recall
External ID
H-0902-2026
Action Date
2026-06-10
Status
Terminated
Category
food
Product Description
My Wife's Slaw Jalapeno Heat, packaged in 8 oz. and 16 oz. glass mason jars with metal lids/bands, MyWifeslaw.web.app, Zanesville, Ohio. Ingredients: Cabbage, Sugar, Vinegar, Mustard, Carrots, Onion, Bell Pepper, Salt, Black Pepper, Cayenne Pepper, Jalapenos, Red Pepper Flakes.
Lot/Code Info: No codes applied
Quantity Affected: 10 individual units (TOTAL)
Reason for Recall
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
Distribution
Products distributed directly to end consumers in AL, OH, TX, WV.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-05-05
Company
Zanesville, OH
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 166 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Jesse Withrow has 2 FDA actions in our database, including 2 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 (Jesse Withrow) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Jesse Withrow have FDA actions?
Jesse Withrow has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0902-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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