Wickles Relish 16oz Jars: Wrong Label Hazard
Magnolia Vegetable Processors recalls Wickles Relish 16oz glass jars with wrong labels. Check lot numbers for affected items.
Lower-risk recall
Wrong Label applied to Product.
Contact the company
What happened, in plain English
Magnolia Vegetable Processors is recalling Wickles Relish 16oz glass jars due to a wrong label applied to the product. This could lead to confusion about the product's contents or expiration date, but it does not pose a direct safety risk. Read more at govinfonow.com/recall/14308-wickles-relish-16oz-jars-wrong-label-hazard.
Source Summary by GovInfoNow · govinfonow.com/recall/14308-wickles-relish-16oz-jars-wrong-label-hazard · Updated October 4, 2026 · FDA enforcement record: FDA #F-0859-2021
Cite this page
“Wickles Relish 16oz Jars: Wrong Label Hazard.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/14308-wickles-relish-16oz-jars-wrong-label-hazard. Based on FDA recall #F-0859-2021 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0859-2021%22&limit=1).
Why it’s dangerous
The wrong label on the jars could cause confusion about the product's contents or expiration date. This might lead to using the product past its best by date or misidentifying the product, but it does not cause physical harm.
Who’s affected
Owners of Wickles Relish 16oz glass jars with lot number 2001210406 or product number 2001 are affected. Consumers who purchased these jars from stores selling the product are most at risk.
How to tell if you have this one
Check for lot number 2001210406 and product number 2001 on the jar's label. The product was sold with a best by date of 04/06/24.
- Brand
Magnolia Vegetable Processors- Category
Food
What to do — step by step
Check Label
Look for lot number 2001210406 and product number 2001 on the jar's label.
Where it went and when
Where it was distributed
Distributed in 8 states.
FDA distribution: “Distributed to the following states: IL, KY, LA, ME, MD, NC, PA, VA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Illinois, Kentucky, Louisiana, Maine, Maryland, North Carolina, Pennsylvania, Virginia.
Recall timeline
FDA terminated this recall 29 days after the firm started it.
- Firm started the recall
- FDA classified it Class III
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-0859-2021 (July 20, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0859-2021 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.