American Outdoor Products, Inc. Recall: An almond allergen is missing from the Contains statement. The ingredient list on the package lists Almonds as an ingredient, however the Contains statement did not include Almond.

🇺🇸 United States

1. April 25, 2023 - Recall initiated
2. May 31, 2023 - Reported by source
3. July 12, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0897-2023

Event ID

92169

Status

Terminated

Classification

Class II

Company

American Outdoor Products, Inc.

Product description

Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143

Quantity

61,101 pouches

Reason

An almond allergen is missing from the Contains statement. The ingredient list on the package lists Almonds as an ingredient, however the Contains statement did not include Almond.

Recall initiation date

April 25, 2023

Report date

May 31, 2023

Classification date

Not published in this source record

Termination date

July 12, 2023

Distribution pattern

Alabama Alaska Arizona Arkansas California Colorado Connecticut Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana

UPC, lot, and code information

UPC -048143026143; 30 DEC 24 19 JAN 25 27 JAN 25 01 FEB 25 15 FEB 25 01 MAR 25 17 MAR 25 04 MAY 25 11 MAY 25 13 MAY 25 26 May 25 27 MAY 25 17 JUN 25 14 JUN 25 29 JUN 25 01 JUL 25 22 JUL 25 02 AUG 25 08 AUG 25 18 AUG 25 01 SEP 25 02 SEP 25 14 SEP 25 20 SEP 25

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: American Outdoor Products, Inc.

Other recalls from American Outdoor Products, Inc.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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