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Class II: temporary or reversible health riskTerminated

American Importing Product label: Amport Foods Recall

Product label: Amport Foods, Granola, Cinnamon Crunch, 22 oz (1 lb, 6 0z), UPC 0 7172…

American Importing Co, Inc · Minneapolis, MN

Risk level
Class II
Reported by FDA
Jun 25, 2014
Recall ID
F-2034-2014
Check your lot numberHow we source this data

Summary

American Importing recalled Product label: Amport Foods starting May 2, 2014. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2034-2014 on Jun 25, 2014. Reason: 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. Status: Terminated.

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.

Product description

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.

Lot numbers, UPCs & expiration codes

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

Where it was sold

NY, ND, MN, WI, CA.

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-2034-2014
Classification
Class II
Status
Terminated
Recall initiated
May 2, 2014
FDA report date
Jun 25, 2014
Quantity
229 cases
Recall type
Voluntary: Firm initiated
Recalling firm
American Importing Co, Inc

Original FDA data

Every field from FDA enforcement report F-2034-2014, exactly as published.

Show all FDA fields
City
Minneapolis
State
MN
Status
Terminated
Country
United States
Event ID
68408
Address
550 Kasota Ave SE
Code information
Best By 03-26-15. Lot Code: 085x418.
Postal code
55414-2811
Report date
Jun 25, 2014
Product type
Food
Recall number
F-2034-2014
Classification
Class II
Recalling firm
American Importing Co, Inc
Product quantity
229 cases
Termination date
Aug 28, 2014
Reason for recall
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.
Voluntary / mandated
Voluntary: Firm initiated
Product description
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.
Distribution pattern
NY, ND, MN, WI, CA.
Recall initiation date
May 2, 2014
Initial firm notification
Press Release
Center classification date
Jun 16, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2034-2014, published Jun 25, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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