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Class I: serious health riskTerminated

Brand New Energy EphBurn 25 Recall

EphBurn 25, 90 count bottle with red capsules

Brand New Energy, LLC · Burbank, CA

Risk level
Class I
Reported by FDA
Apr 24, 2013
Recall ID
F-1325-2013
Check your lot numberHow we source this data

Summary

Brand New Energy recalled EphBurn 25 starting Aug 30, 2012. The FDA classified it as Class I (serious health risk) and published enforcement report F-1325-2013 on Apr 24, 2013. Reason: Brand New Energy is recalling all lot codes of EphBurn 25 because it may contain ephedrine alkaloids, making it an unapproved drug. Status: Terminated.

Why it was recalled

Brand New Energy is recalling all lot codes of EphBurn 25 because it may contain ephedrine alkaloids, making it an unapproved drug.

Product description

EphBurn 25, 90 count bottle with red capsules

Lot numbers, UPCs & expiration codes

all lot codes, no UPC codes

Where it was sold

ID, NY, KS, CO,

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-1325-2013
Classification
Class I
Status
Terminated
Recall initiated
Aug 30, 2012
FDA report date
Apr 24, 2013
Quantity
1000 units
Recall type
Voluntary: Firm initiated
Recalling firm
Brand New Energy, LLC

Original FDA data

Every field from FDA enforcement report F-1325-2013, exactly as published.

Show all FDA fields
City
Burbank
State
CA
Status
Terminated
Country
United States
Event ID
63060
Address
3424 W. Magnolia Blvd.
Code information
all lot codes, no UPC codes
Postal code
91505
Report date
Apr 24, 2013
Product type
Food
Recall number
F-1325-2013
Classification
Class I
Recalling firm
Brand New Energy, LLC
Product quantity
1000 units
Termination date
Apr 18, 2013
Reason for recall
Brand New Energy is recalling all lot codes of EphBurn 25 because it may contain ephedrine alkaloids, making it an unapproved drug.
Voluntary / mandated
Voluntary: Firm initiated
Product description
EphBurn 25, 90 count bottle with red capsules
Distribution pattern
ID, NY, KS, CO,
Recall initiation date
Aug 30, 2012
Initial firm notification
Press Release
Center classification date
Apr 17, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1325-2013, published Apr 24, 2013. View the source record (openFDA) · FDA enforcement reports

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

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