Julie's Real JR Bar Cinnamon Vanilla Bean Grain-Free Granola Bar, Net Wt 1.4 oz (40g), UPC 857628006699, packaged and so
Summary
The FDA issued a Class II for Julie's Real JR Bar Cinnamon Vanilla Bean Grain-Free Granola Bar, Net Wt 1.4 oz by Julie's Real Foods LLC. Reason: Possible presence of foreign material (metal).
Details
Source
Food Recall
External ID
F-0938-2023
Action Date
2023-05-31
Status
Terminated
Category
food
Product Description
Julie's Real JR Bar Cinnamon Vanilla Bean Grain-Free Granola Bar, Net Wt 1.4 oz (40g), UPC 857628006699, packaged and sold in a 6 Pack Box to consumers, sold as a Master Case of 6, 6 Pack Boxes to retailer and distributor
Lot/Code Info: Lot 0522; Best By Dates 5/2/2023, 5/3/2023, 5/4/2023
Quantity Affected: 22,290 boxes
Reason for Recall
Possible presence of foreign material (metal)
Distribution
Nationwide throughout the US
Type: Voluntary: Firm initiated
Recall Initiated: 2023-05-10
Company
Dallas, TX
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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Julie's Real Foods 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 (Julie's Real Foods LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Julie's Real Foods LLC have FDA actions?
Julie's Real Foods 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-0938-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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