FDA recall, , Moderate risk
My Wife's Slaw
My Wife's Slaw was produced without an approved inspection, so its safety could not be verified.
Recall ended Jun 26, 2026. Still check yours.
Summary by Recall Canary from the FDA notice
What happened
Jesse Withrow of Zanesville, Ohio, is recalling My Wife's Slaw and My Wife's Slaw Jalapeno Heat coleslaws sold in 8 oz. and 16 oz. glass mason jars with metal lids/bands. The products were manufactured and distributed without the benefit of an approved food establishment inspection, and the required regulatory safety parameters could not be verified. The recall was announced May 5, 2026, and added to the FDA's Enforcement Report on June 2, 2026.
The products were distributed directly to end consumers in Alabama, Ohio, Texas, and West Virginia. The recall covers the Original and Jalapeno Heat flavors, each with 10 individual units total.
2 photos
What to do
If you have one of these products:
- Consumers with questions regarding this recall can contact Jesse Withrow at 740-280-2141 or mywifeslaw@
outlook.com. - Discontinue use immediately. - Dispose of product safely.
Is yours affected?
Compare the details below with your product and check the FDA notice to confirm whether it is affected.
My Wife's Slaw Jalapeno Heat
Product details from the notice
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.
My Wife's Slaw
Product details from the notice
My Wife's Slaw, 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.
Recall details
- Company began the recall
- Sold in
Products distributed directly to end consumers in Alabama, Ohio, Texas, West Virginia.
- Company
- Jesse WithrowZanesville, Ohio
- Risk
Moderate risk
Eating it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98943
- Recall numbers
- H-0901-2026 to H-0902-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall · Announced by the company
Listed on Recall Canary
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Recall ended
Archived
Summary updated
