RecallHawk

Almond Joy Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice cream bars . 6

Unilever North America Supply Chain Company, LLC

Summary

The FDA issued a recall for Almond Joy Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing by Unilever North America Supply Chain Company, LLC. Reason: Inaccurate Nutrition Facts information listed on product.

Details

Source

Food Recall

External ID

125b9787-c977-4c8e-b079-1199bd9d7515

Action Date

2026-09-30

Status

Ongoing

Category

food

Product Description

Almond Joy Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice cream bars . 6 bars per carton. Keep frozen

Lot/Code Info: APR0927XS3 APR1027XS3 JUN1527XS3 JUN1627XS3 AUG1127XS3 AUG1227XS3 AUG1327XS3 AUG1427XS3 OCT0827XS3 OCT0927XS3 OCT3027XS3 OCT3127XS3 DEC0127XS3 DEC0227XS3 DEC0327XS3 DEC0427XS3 JAN1228XS3 JAN1328XS3 JAN1428XS3 JAN1528XS3

Quantity Affected: 63,226 cases

Reason for Recall

Inaccurate Nutrition Facts information listed on product

Distribution

The adulterated product was distributed to the following states: AZ,MD,NM,WI,CO,HI,MO, IA, GA, SC, WA,PA, IL, CA, OR, TX,FL, NH,LA,KS,MS, OK,MO,MN, MI, TN, NY, NV, UT, OH, NJ, AK,VA, AL, ME

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-11

Context & Analysis

This is a unclassified recall.

This was one of 58 food recalls issued in the same week, part of 82 food-related FDA actions this month.

Unilever North America Supply Chain Company, LLC has 2 FDA actions in our database, including 2 recalls.

Frequently Asked Questions

What is a FDA recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Unilever North America Supply Chain Company, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Unilever North America Supply Chain Company, LLC have FDA actions?

Unilever North America Supply Chain Company, 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 "125b9787-c977-4c8e-b079-1199bd9d7515" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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