RecallHawk
Class II Recall

Trader Joes Dark Chocolate Almond Butter Cup, 1.4 oz. (2-20-gram cups per pack), PVC Pouch, 72 packs per case; 2 cups pe

Bazzini LLC

Summary

The FDA issued a Class II for Trader Joes Dark Chocolate Almond Butter Cup, 1.4 oz. (2-20-gram cups per pack), by Bazzini LLC. Reason: Potential undeclared peanut allergen..

Details

Source

Food Recall

External ID

F-0772-2021

Action Date

2021-07-21

Status

Terminated

Category

food

Product Description

Trader Joes Dark Chocolate Almond Butter Cup, 1.4 oz. (2-20-gram cups per pack), PVC Pouch, 72 packs per case; 2 cups per pack .

Lot/Code Info: Apr 05 2022 1B095 Apr 05 2022 2B095 Apr 06 2022 1B096 Apr 06 2022 2B096 Apr 07 2022 1B097 Apr 07 2022 2B097

Quantity Affected: 2816 Cases

Reason for Recall

Potential undeclared peanut allergen.

Distribution

The recall product was distributed to the following states, PA, IL, CT, CA, WA, TX FL

Type: Voluntary: Firm initiated

Recall Initiated: 2021-06-21

Company

Bazzini LLC

Allentown, PA

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

Bazzini LLC has 5 FDA actions in our database, including 5 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 (Bazzini LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bazzini LLC have FDA actions?

Bazzini LLC has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0772-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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