Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has UP
Summary
The FDA issued a Class II for Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individ by Betty Lou's Inc. Reason: Undeclared Sesame.
Details
Source
Food Recall
External ID
F-0301-2024
Action Date
2023-11-01
Status
Terminated
Category
food
Product Description
Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has UPC 0 16073 00213 1. There are 12 packages per display box (box UPC 0 16073 00223 0). The label allergens contains statement declares Milk, Peanut, Tree Nuts (Almond, Cashew, Coconut, Hazelnut).
Lot/Code Info: BB 05APR24 hh:mm F6 0053 The code breaks down as: BB 05APR24: Best by Day, Month, Year hh:mm hour and minute of packaging F6 is packaging line identifier. 005: Julian Date of Manufactured Date 3: Last digit of Manufactured Year 0053: Manufactured on January 5th, 2023
Quantity Affected: 5,197 bars
Reason for Recall
Undeclared Sesame
Distribution
Distributed in AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, KY, MA, MI, MT, NV, NY, OH, OK, OR, PA, TN, TX, WA, WI, and WY.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-09
Company
Mcminnville, OR
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 16 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 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 (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-0301-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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