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Class II: temporary or reversible health riskTerminated

El Alteno Raisinettes Dovales 12 oz Recall

El Alteno Raisinettes Dovales 12 oz

El Alteno · Los Angeles, CA

Risk level
Class II
Reported by FDA
Sep 28, 2016
Recall ID
F-2343-2016
Check your lot numberHow we source this data

Summary

El Alteno recalled El Alteno Raisinettes Dovales 12 oz starting Aug 5, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2343-2016 on Sep 28, 2016. Reason: Undeclared milk and soy lecithin. Status: Terminated.

Why it was recalled

Undeclared milk and soy lecithin.

Product description

El Alteno Raisinettes Dovales 12 oz. UPC: 8 20202 00411 4

Lot numbers, UPCs & expiration codes

Exp Date 06/30/2017

Where it was sold

U.S. distribution to the following; CA, AZ, NV. No foreign distribution.

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-2343-2016
Classification
Class II
Status
Terminated
Recall initiated
Aug 5, 2016
FDA report date
Sep 28, 2016
Quantity
20 dozen packages
Recall type
Voluntary: Firm initiated
Recalling firm
El Alteno

Original FDA data

Every field from FDA enforcement report F-2343-2016, exactly as published.

Show all FDA fields
City
Los Angeles
State
CA
Status
Terminated
Country
United States
Event ID
74870
Address
1200 E 8th St
Code information
Exp Date 06/30/2017
Postal code
90021-1514
Report date
Sep 28, 2016
Product type
Food
Recall number
F-2343-2016
Classification
Class II
Recalling firm
El Alteno
Product quantity
20 dozen packages
Termination date
May 10, 2017
Reason for recall
Undeclared milk and soy lecithin.
Voluntary / mandated
Voluntary: Firm initiated
Product description
El Alteno Raisinettes Dovales 12 oz. UPC: 8 20202 00411 4
Distribution pattern
U.S. distribution to the following; CA, AZ, NV. No foreign distribution.
Recall initiation date
Aug 5, 2016
Initial firm notification
E-Mail
Center classification date
Sep 16, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2343-2016, published Sep 28, 2016. View the source record (openFDA) · FDA enforcement reports

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

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