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Class II: temporary or reversible health riskTerminated

Beta Labs Oxyphen XR Recall

Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSU…

Beta Labs · Memphis, TN

Risk level
Class II
Reported by FDA
Sep 3, 2014
Recall ID
F-2398-2014
Check your lot numberHow we source this data

Summary

Beta Labs recalled Oxyphen XR starting Jun 20, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-2398-2014 on Sep 3, 2014. Reason: The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements. Status: Terminated.

Why it was recalled

The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.

Product description

Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599747

Lot numbers, UPCs & expiration codes

Lot #s 200910 and 200911, Exp 10/16

Where it was sold

nationwide and UK

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-2398-2014
Classification
Class II
Status
Terminated
Recall initiated
Jun 20, 2013
FDA report date
Sep 3, 2014
Quantity
5951 units
Recall type
Voluntary: Firm initiated
Recalling firm
Beta Labs

Original FDA data

Every field from FDA enforcement report F-2398-2014, exactly as published.

Show all FDA fields
City
Memphis
State
TN
Status
Terminated
Country
United States
Event ID
65585
Address
2 W GE Patterson Ave Apt 103
Code information
Lot #s 200910 and 200911, Exp 10/16
Postal code
38103-6429
Report date
Sep 3, 2014
Product type
Food
Recall number
F-2398-2014
Classification
Class II
Recalling firm
Beta Labs
Product quantity
5951 units
Termination date
Dec 3, 2014
Reason for recall
The products contain DMAA, also known as 1,3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.
Voluntary / mandated
Voluntary: Firm initiated
Product description
Oxyphen XR, 12 HR / CLINICAL STRENGTH FAT BURNER, 45 FAST ACTING EXTENDED RELEASE CAPSULES, Distributed by Beta Labs, LTD, Newark, DE 19711, UPC 670541599747
Distribution pattern
nationwide and UK
Recall initiation date
Jun 20, 2013
Initial firm notification
Press Release
Center classification date
Aug 27, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-2398-2014, published Sep 3, 2014. View the source record (openFDA) · FDA enforcement reports

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

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