Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143
Summary
The FDA issued a Class II for Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-0 by American Outdoor Products, Inc.. Reason: An almond allergen is missing from the Contains statement. The ingredient list on the package lists Almonds as an ingredient, however the Contains sta.
Details
Source
Food Recall
External ID
F-0897-2023
Action Date
2023-05-31
Status
Terminated
Category
food
Product Description
Backpacker s Pantry Blueberry Peach Crisp, 4.6-ounce, packaged in a pouch, UPC-048143026143
Lot/Code Info: 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
Quantity Affected: 61,101 pouches
Reason for 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.
Distribution
Alabama Alaska Arizona Arkansas California Colorado Connecticut Florida Georgia Hawaii Idaho Illinois Indiana Iowa Kansas Kentucky Louisiana Maine Maryland Massachusetts Michigan Minnesota Mississippi Missouri Montana Nebraska Nevada New Hampshire New Jersey New Mexico New York North Carolina North Dakota Ohio Oklahoma Oregon Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Utah Vermont Virginia Washington West Virginia Wisconsin Wyoming
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-25
Company
Boulder, CO
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 71 food recalls issued in the same week, part of 204 food-related FDA actions this month.
American Outdoor Products, 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 (American Outdoor Products, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does American Outdoor Products, Inc. have FDA actions?
American Outdoor Products, 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-0897-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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