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Class II: temporary or reversible health riskTerminated

Sokol and Solo Almond Paste Recall

Solo Almond Paste, 6/7 LB

Sokol and Co · Countryside, IL

Risk level
Class II
Reported by FDA
Nov 16, 2016
Recall ID
F-0427-2017
Check your lot numberHow we source this data

Summary

Sokol and recalled Solo Almond Paste starting Oct 21, 2016. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-0427-2017 on Nov 16, 2016. Reason: Pieces of plastic and metal discovered within product. Status: Terminated.

Why it was recalled

Pieces of plastic and metal discovered within product.

Product description

Solo Almond Paste, 6/7 LB. Cans, Net Weight: 42 LBS. (19.09 KG.)

Lot numbers, UPCs & expiration codes

Lot: 16278

Where it was sold

MA, MI, TX

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-0427-2017
Classification
Class II
Status
Terminated
Recall initiated
Oct 21, 2016
FDA report date
Nov 16, 2016
Quantity
486 cans
Recall type
Voluntary: Firm initiated
Recalling firm
Sokol and Co

Original FDA data

Every field from FDA enforcement report F-0427-2017, exactly as published.

Show all FDA fields
City
Countryside
State
IL
Status
Terminated
Country
United States
Event ID
75550
Address
5315 Dansher Rd
Code information
Lot: 16278
Postal code
60525-3101
Report date
Nov 16, 2016
Product type
Food
Recall number
F-0427-2017
Classification
Class II
Recalling firm
Sokol and Co
Product quantity
486 cans
Termination date
Apr 22, 2019
Reason for recall
Pieces of plastic and metal discovered within product.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Solo Almond Paste, 6/7 LB. Cans, Net Weight: 42 LBS. (19.09 KG.)
Distribution pattern
MA, MI, TX
Recall initiation date
Oct 21, 2016
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Nov 10, 2016

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-0427-2017, published Nov 16, 2016. View the source record (openFDA) · FDA enforcement reports

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

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