Class IITerminated in FDA datasetRecall initiated Aug 22, 2024

American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic…

Recalling firm: American Outdoor Products, Inc.

Why it was recalled

Elevated levels of lead

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jan 17, 2025.

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Compare the exact product and package details with the label you have.

ProductAmerican Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually or in 6, 12, 40, or 160 count cases. One unit is also included in the Outerspace Survival Dessert Kit. Shelf stable.
Package size0.5oz
UPC048143300106

FDA code information

UPC: 048143300106 Lot numbers: 125130, 125133, 20240509-6, 20240509-7, 20240514-6, 20240524-2, 20240607-2, 20240711-2, 20240719-2, 20240723-2, 20240807-2, 20240808-2, and 20240816-2 Still on site Best By Dates: 12APR27, 09MAY276, 09MAY277, 14MAY276, 24MAY272, 07JUN272, 11JUL272, 19JUL272, 23JUL272, 07AUG272

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually or in 6, 12, 40, or 160 count cases. One unit is also included in the Outerspace Survival Dessert Kit. Shelf stable.

Extracted codes and context

TypeCode / valueContext
UPC048143300106UPC: 048143300106 Lot numbers: 125130, 125133, 20240509-6, 20240509-7, 20240514-6, 20240524-2, 20240607-2, 20240711-2, 20240719-2, 20240

Original FDA recall reason

Elevated levels of lead

Recall details

Recall number
F-1807-2024
Event ID
95255
FDA status
Terminated
Initiated
Aug 22, 2024
Reported
Sep 18, 2024
Classified
Sep 12, 2024
Terminated
Jan 17, 2025
Quantity
14,235 units
Location
Boulder, CO, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Nationwide: Alabama, California, Colorado, Delaware, Florida, Georgia, Hawaii, Illinois, Indiana, Kansas, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Nevada, New Jersey, New York, North Carolina, Ohio, Oklahoma, Pennsylvania, Tennessee, Texas, Vermont, Virginia, Washington, Wisconsin, Washington DC

FDA source record · F-1807-2024

Data updated September 16, 2026. View official FDA data ↗

Follow official FDA and manufacturer guidance.