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Class II: temporary or reversible health riskTerminated

El Alteno Coconut Shredded Coconut 8 oz Recall

El Alteno Coconut Shredded Coconut 8 oz

El Alteno · Los Angeles, CA

Risk level
Class II
Reported by FDA
Sep 28, 2016
Recall ID
F-2344-2016
Check your lot numberHow we source this data

Summary

El Alteno recalled El Alteno Coconut Shredded Coconut 8 oz starting Aug 5, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2344-2016 on Sep 28, 2016. Reason: Undeclared sulfites. Status: Terminated.

Why it was recalled

Undeclared sulfites

Product description

El Alteno Coconut Shredded Coconut 8 oz. UPC: 8 20202 00362 9

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-2344-2016
Classification
Class II
Status
Terminated
Recall initiated
Aug 5, 2016
FDA report date
Sep 28, 2016
Quantity
53 dozen packages
Recall type
Voluntary: Firm initiated
Recalling firm
El Alteno

Original FDA data

Every field from FDA enforcement report F-2344-2016, exactly as published.

Show all FDA fields
City
Los Angeles
State
CA
Status
Terminated
Country
United States
Event ID
74869
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-2344-2016
Classification
Class II
Recalling firm
El Alteno
Product quantity
53 dozen packages
Termination date
May 10, 2017
Reason for recall
Undeclared sulfites
Voluntary / mandated
Voluntary: Firm initiated
Product description
El Alteno Coconut Shredded Coconut 8 oz. UPC: 8 20202 00362 9
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-2344-2016, published Sep 28, 2016. View the source record (openFDA) · FDA enforcement reports

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

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