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Class I: serious health riskTerminated

NuGo Slim Espresso Recall

NuGo Slim Espresso, 1

NuGo Nutrition HQ · Oakmont, PA

Risk level
Class I
Reported by FDA
Aug 28, 2013
Recall ID
F-1833-2013
Check your lot numberHow we source this data

Summary

NuGo Nutrition HQ recalled NuGo Slim Espresso starting Mar 28, 2013. The FDA classified it as Class I (serious health risk) and published enforcement report F-1833-2013 on Aug 28, 2013. Reason: Product may contain undeclared milk product. Status: Terminated.

Why it was recalled

Product may contain undeclared milk product

Product description

NuGo Slim Espresso, 1.59 oz (45g) Non-Dairy

Lot numbers, UPCs & expiration codes

Best By date ending in 2012 and 2013 UPC 69153520902 (box) UPC 69153520901 (bar)

Where it was sold

Nationwide and Canada.

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-1833-2013
Classification
Class I
Status
Terminated
Recall initiated
Mar 28, 2013
FDA report date
Aug 28, 2013
Quantity
N/A
Recall type
Voluntary: Firm initiated
Recalling firm
NuGo Nutrition HQ

Original FDA data

Every field from FDA enforcement report F-1833-2013, exactly as published.

Show all FDA fields
City
Oakmont
State
PA
Status
Terminated
Country
United States
Event ID
64666
Address
520 2nd St
Code information
Best By date ending in 2012 and 2013 UPC 69153520902 (box) UPC 69153520901 (bar)
Postal code
15139-2025
Report date
Aug 28, 2013
Product type
Food
Recall number
F-1833-2013
Classification
Class I
Recalling firm
NuGo Nutrition HQ
Termination date
Aug 26, 2014
Reason for recall
Product may contain undeclared milk product
Voluntary / mandated
Voluntary: Firm initiated
Product description
NuGo Slim Espresso, 1.59 oz (45g) Non-Dairy
Distribution pattern
Nationwide and Canada.
Recall initiation date
Mar 28, 2013
Initial firm notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Center classification date
Aug 19, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1833-2013, published Aug 28, 2013. View the source record (openFDA) · FDA enforcement reports

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

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