Wickles Relish recall
Recalled by Magnolia Vegetable Processors · Brundidge, AL, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Wrong Label applied to Product.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
Wickles Relish 16oz glass jars - 6 jars per case
Quantity: 2904 cases
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.
Lot No. 2001210406 Product No. 2001 Best By 04/06/24
Where it was sold
Illinois Kentucky Louisiana Maryland Maine North Carolina Pennsylvania Virginia
FDA's distribution note: Distributed to the following states: IL, KY, LA, ME, MD, NC, PA, VA
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. 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
- Magnolia Vegetable Processors
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jul 20, 2021
- In FDA report of
- Aug 18, 2021
- Terminated
- Aug 18, 2021
- FDA recall number
- F-0859-2021 · event 88316
- Official record
- FDA enforcement report search