RecallHawk
Class II Recall

JLM Sesame Sticks Mix in clear plastic 11oz. tub UPC 094776081646 12 retail units per case

JLM Manufacturing LLC

Summary

The FDA issued a Class II for JLM Sesame Sticks Mix in clear plastic 11oz. tub UPC 094776081646 12 retail uni by JLM Manufacturing LLC. Reason: Undeclared cashew.

Details

Source

Food Recall

External ID

F-0144-2023

Action Date

2022-11-16

Status

Terminated

Category

food

Product Description

JLM Sesame Sticks Mix in clear plastic 11oz. tub UPC 094776081646 12 retail units per case

Lot/Code Info: Lots 08202209B 13202209B Best By 03/07/23 03/12/23

Quantity Affected: 307 cases

Reason for Recall

Undeclared cashew

Distribution

Florida, Gerogia, Illinois, Indiana, Kentucky, Maryland, Michigan, Minnesota, Missouri, North Carolina, New York, Ohio, Oklahoma, Pennsylvania, Texas, Tennessee, Wisconsin, West Virginia.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-10-03

Company

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 66 food recalls issued in the same week, part of 204 food-related FDA actions this month.

JLM Manufacturing LLC has 2 FDA actions in our database, including 2 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 (JLM Manufacturing LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does JLM Manufacturing LLC have FDA actions?

JLM Manufacturing LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0144-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions