“Lipari Roasted Salted Pecan Halves Recall: Product Mislabeled as Pecans.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/10377-lipari-roasted-salted-pecan-halves-recall-product-mislabeled-as-pecans. Based on FDA recall #F-0002-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0002-2024%22&limit=1).
The FDA announced on Sept. 6, 2023, that Lipari Foods Operating Company LLC voluntarily recalled JLM Roasted Salted Pecan Halves because the product contains filberts instead of the labeled pecans. The agency stated the recall is voluntary and initiated by the firm.
How to tell if you have it
Brand: Lipari
Product: JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale case
Lipari number: 368729
UPC: 094776110049
Lot#: 09202306A
The hazard
The top label says Roasted Salted Pecan Halves, but the product is actually filberts or hazelnuts. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Lipari Foods Operating Company LLC has had 11 other recalls on record since Dec. 11, 2018. Other recent recalls of similar products include Lipari Foods Dark Chocolate Nonpareils Recall (June 18, 2025), Premo King Club Footlong 11.5oz Recall (June 27, 2024), and IO Inspired Organics Organic Raw Walnuts Recall (Sept. 9, 2023). Other recent recalls of similar products include Albertsons Yellow Fudge Pecan Recall (May 6, 2026), Albertsons Thumbprint Snack Cheeze Susans Recall (May 6, 2026), and Albertsons Cake Craving Carrot Recall (May 6, 2026).
How to tell if you have this one
Check for the Lipari number 368729 or UPC 094776110049 on the product. The product comes in a 10oz clear plastic container with 12 pieces per case.
Brand
Lipari
Product
JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale case. Lipari number 368729, UPC
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the Lipari number 368729 or UPC 094776110049 on the product label.
Where it went and when
Where it was distributed
Distributed in 8 states.
Listed by the agency
Not listed
FDA distribution: “MI OH IL PA FL WV IN MT” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Illinois, Indiana, Michigan, Montana, Ohio, Pennsylvania, West Virginia.
Recall timeline
FDA terminated this recall 3 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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-0002-2024 (September 6, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0002-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 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.