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Class I: serious health riskTerminated

Houdini Alfasi Cabernet Kosher Selection Basket #810 Recall

Alfasi Cabernet Kosher Selection Basket #810

Houdini Inc. · Fullerton, CA

Risk level
Class I
Reported by FDA
Feb 8, 2017
Recall ID
F-1411-2017
Check your lot numberHow we source this data

Summary

Houdini recalled Alfasi Cabernet Kosher Selection Basket #810 starting Dec 9, 2016. The FDA classified it as Class I (serious health risk) and published enforcement report F-1411-2017 on Feb 8, 2017. Reason: Potential Salmonella contamination. Status: Terminated.

Why it was recalled

Potential Salmonella contamination.

Product description

Alfasi Cabernet Kosher Selection Basket #810

Lot numbers, UPCs & expiration codes

Lot #LC444152

Where it was sold

U.S. distribution to the following; nationwide including Puerto Rico.

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-1411-2017
Classification
Class I
Status
Terminated
Recall initiated
Dec 9, 2016
FDA report date
Feb 8, 2017
Quantity
31 baskets
Recall type
Voluntary: Firm initiated
Recalling firm
Houdini Inc.

Original FDA data

Every field from FDA enforcement report F-1411-2017, exactly as published.

Show all FDA fields
City
Fullerton
State
CA
Status
Terminated
Country
United States
Event ID
75933
Address
4225 N Palm St
Code information
Lot #LC444152
Postal code
92835-1045
Report date
Feb 8, 2017
Product type
Food
Recall number
F-1411-2017
Classification
Class I
Recalling firm
Houdini Inc.
Product quantity
31 baskets
Termination date
Mar 1, 2017
Reason for recall
Potential Salmonella contamination.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Alfasi Cabernet Kosher Selection Basket #810
Distribution pattern
U.S. distribution to the following; nationwide including Puerto Rico.
Recall initiation date
Dec 9, 2016
Initial firm notification
Letter
Center classification date
Feb 1, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1411-2017, published Feb 8, 2017. View the source record (openFDA) · FDA enforcement reports

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

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