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Class II: temporary or reversible health riskTerminated

Colony Brands Lobster Bisque Recall

Lobster Bisque, product 45036

Colony Brands, Inc. · Monroe, WI

Risk level
Class II
Reported by FDA
Jan 22, 2014
Recall ID
F-1386-2014
Check your lot numberHow we source this data

Summary

Colony Brands recalled Lobster Bisque starting Dec 5, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1386-2014 on Jan 22, 2014. Reason: Lobster Bisque contains undeclared wheat allergen. Status: Terminated.

Why it was recalled

Lobster Bisque contains undeclared wheat allergen.

Product description

Lobster Bisque, product 45036. Net WT 4.0 lbs. Keep Frozen.

Lot numbers, UPCs & expiration codes

Lot number 3418130

Where it was sold

OK, TX, NY, ND, FL, PA, CA, CO, NV, AL, MI, AR, MA.

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-1386-2014
Classification
Class II
Status
Terminated
Recall initiated
Dec 5, 2013
FDA report date
Jan 22, 2014
Quantity
19 units
Recall type
Voluntary: Firm initiated
Recalling firm
Colony Brands, Inc.

Original FDA data

Every field from FDA enforcement report F-1386-2014, exactly as published.

Show all FDA fields
City
Monroe
State
WI
Status
Terminated
Country
United States
Event ID
67051
Address
1112 7th Ave
Code information
Lot number 3418130
Postal code
53566-1364
Report date
Jan 22, 2014
Product type
Food
Recall number
F-1386-2014
Classification
Class II
Recalling firm
Colony Brands, Inc.
Product quantity
19 units
Termination date
Aug 21, 2017
Reason for recall
Lobster Bisque contains undeclared wheat allergen.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Lobster Bisque, product 45036. Net WT 4.0 lbs. Keep Frozen.
Distribution pattern
OK, TX, NY, ND, FL, PA, CA, CO, NV, AL, MI, AR, MA.
Recall initiation date
Dec 5, 2013
Initial firm notification
Letter
Center classification date
Jan 10, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1386-2014, published Jan 22, 2014. View the source record (openFDA) · FDA enforcement reports

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

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