JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale case. Lipari number 368729, UPC 0947761
Summary
The FDA issued a Class II for JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale by Lipari Foods Operating Company, LLC.. Reason: Top label says Roasted Salted Pecan Halves, but product is actually filberts / hazelnuts.
Details
Source
Food Recall
External ID
F-0002-2024
Action Date
2023-10-11
Status
Terminated
Category
food
Product Description
JLM Roasted Salted Pecan Halves, 10oz clear plastic container, 12 per wholesale case. Lipari number 368729, UPC 094776110049
Lot/Code Info: Lot# 09202306A
Quantity Affected: 98 cases
Reason for Recall
Top label says Roasted Salted Pecan Halves, but product is actually filberts / hazelnuts
Distribution
MI OH IL PA FL WV IN MT
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-06
Company
Warren, MI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 163 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lipari Foods Operating Company, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lipari Foods Operating Company, LLC. have FDA actions?
Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0002-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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