My Wife's Slaw
Reason Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
My Wife's Slaw Jalapeno Heat recall
Recalled by Jesse Withrow · Zanesville, OH, United States
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Why it was recalled
Product was manufactured and distributed without the benefit of an approved food establishment inspection and the required regulatory safety parameters could not be verified.
See the recall's own reason text for the specifics. All other reasons recalls.
What was recalled
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.
Quantity: 10 individual units (TOTAL)
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
No codes applied
Where it was sold
Alabama Ohio Texas West Virginia
FDA's distribution note: Products distributed directly to end consumers in AL, OH, TX, WV.
Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Jesse Withrow
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- May 5, 2026
- In FDA report of
- Jun 10, 2026
- Terminated
- Jun 26, 2026
- FDA recall number
- H-0902-2026 · event 98943
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.