Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds, shelf-stable, 12-month shelf life, 1.
Summary
The FDA issued a Class I for Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seed by Betty Lou's Inc. Reason: Undeclared sesame. Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds product containing sesame was packaged and labeled with Paleo.
Details
Source
Food Recall
External ID
F-1366-2023
Action Date
2023-08-16
Status
Terminated
Category
food
Product Description
Betty Lou's Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds, shelf-stable, 12-month shelf life, 1.5 oz (42g) package and 12/1.5 oz. packages per display box. Packages are sold individually (UPC 0 1607352146 5) or packaged into 12-ct display box (UPC 0 1607352146 2).
Lot/Code Info: BB 08MAY24 hh:mm F5 1283 Best by Day, Month, Year hh:mm hour and minute of packaging F5 is packaging line identifier. 128: Julian Date of Manufactured Date 3: Last digit of Manufactured Year 1282: Manufactured on May 8th, 2023.
Quantity Affected: 1174 bars
Reason for Recall
Undeclared sesame. Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds product containing sesame was packaged and labeled with Paleo Java Nuts About Energy Balls with Cacao, Coffee & Pumpkin Seeds labels that did not declare sesame.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2023-07-06
Company
Mcminnville, OR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 102 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Betty Lou's Inc has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
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 (Betty Lou's Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Betty Lou's Inc have FDA actions?
Betty Lou's Inc 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-1366-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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