Fresh Recalls

FDANot Yet Classified · Food · FDA event 99757; recall number pending · Recalled September 30, 2026

Almond Joy Ice Cream Bar recall — Unilever North America Supply Chain Company, LLC

Agency report date: September 30, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
Almond Joy Ice Cream Bar
Company / brand
Unilever North America Supply Chain Company
Lot / serial / date codes
APR0927XS3 APR1027XS3 JUN1527XS3 JUN1627XS3 AUG1127XS3 AUG1227XS3 AUG1327XS3 AUG1427XS3 OCT0827XS3 OCT0927XS3 OCT3027XS3 OCT3127XS3 DEC0127XS3 DEC0227XS3 DEC0327XS3 DEC0427XS3 JAN1228XS3 JAN1328XS3 JAN1428XS3 JAN1528XS3
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
Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Inaccurate Nutrition Facts information listed on product

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Affected product: Almond Joy Ice Cream Bar recall status

3. Open the official notice or contact

Official recall ID
Not yet assigned by the FDA — identified by FDA event ID 99757
Brand
All Unilever North America Supply Chain Company recalls
Classification
Not Yet Classified
Units affected
63,226 cases
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Englewood Cliffs, NJ, United States
Firm address
700 Sylvan Ave, 07632-3113

Identifying details (verbatim from the notice)

Product codes / lots
APR0927XS3 APR1027XS3 JUN1527XS3 JUN1627XS3 AUG1127XS3 AUG1227XS3 AUG1327XS3 AUG1427XS3 OCT0827XS3 OCT0927XS3 OCT3027XS3 OCT3127XS3 DEC0127XS3 DEC0227XS3 DEC0327XS3 DEC0427XS3 JAN1228XS3 JAN1328XS3 JAN1428XS3 JAN1528XS3
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
Firm notified the public via
E-Mail
FDA event ID
99757
Recall initiated
August 11, 2026
FDA report date
September 30, 2026

Related food recall checkers

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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