RecallHawk
Class II Recall

Stabilyze Sugar Stable Dark Chocolate Peanut Butter, 50g (1.76 oz), sold individual package or box. Each package has UP

Betty Lou's Inc

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

Betty Lou's Inc

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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