Class IITerminated in FDA datasetMay 2, 2014

Product label: Amport Foods, Granola, Cinnamon Crunch

Recalling firm: American Importing Co, Inc

Why it was recalled

American Importing Co, Inc is voluntarily recalling a limited number of packages of a single lot of Cinnamon Crunch Granola because they may contain undeclared almonds. People who have an allergy or sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product. No adverse reactions or illnesses have been reported to date.

Check the codes ↓

The exact product

Product label: Amport Foods, Granola, Cinnamon Crunch, 22 oz (1 lb, 6 0z), UPC 0 71725 72511 0, Best BY 03-26-15, Ingredients: wheat flakes, oat flakes , brown sugar, sugar, coconut oil, coconut, wheat flour, cinnamon, honey, natural vanilla, sea salt. Allergy Information: This product is produced on packaging equipment shared with peanut and tree nut products. Case label: Stock No. 3250420 8/22 oz, Amport Vanilla Almond Granola, Best by 3-26-15, 085X418, UPC 3 00 71725 72512 8.

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Best By 03-26-15. Lot Code: 085x418.

TypeCode / valueContext
UPC071725725110roduct label: Amport Foods, Granola, Cinnamon Crunch, 22 oz (1 lb, 6 0z), UPC 0 71725 72511 0, Best BY 03-26-15, Ingredients: wheat flakes, oat flakes , brown sugar, sugar, coconut oil, coconut, wheat flour, cinna
best by03-26-15Best By 03-26-15. Lot Code: 085x418.
best by03-26-15ds, Granola, Cinnamon Crunch, 22 oz (1 lb, 6 0z), UPC 0 71725 72511 0, Best BY 03-26-15, Ingredients: wheat flakes, oat flakes , brown sugar, sugar, coconut oil, coconut, wheat flour, cinnamon, honey, natura
best by3-26-15 Case label: Stock No. 3250420 8/22 oz, Amport Vanilla Almond Granola, Best by 3-26-15, 085X418, UPC 3 00 71725 72512 8.

Recall details

Recall number
F-2034-2014
Event ID
68408
FDA status
Terminated
Initiated
May 2, 2014
Reported
Jun 25, 2014
Classified
Jun 16, 2014
Terminated
Aug 28, 2014
Quantity
229 cases
Location
Minneapolis, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

NY, ND, MN, WI, CA.

FDA source record · F-2034-2014

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

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.