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RECALL RECORD — CLASS IIRecall closedF-2398-2014/FDA enforcement
Beta Labs·Food·Jun 20, 2013

Oxyphen Xr, 12 Hr / Clinical Strength Fat Burner, 45 Fast Acting Extended Release Capsules, …

What you need to know

Class II

  • What happened

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

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice.

Recall closed · classified by the FDANationwide (US)More food

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Match before you discard

Product identification

Source: FDA FOOD

Brand nameBeta Labs
Recalling firmBeta LabsMemphis, TN, United States
UPC / barcodes
6 70541 59974 7
Lot / date codes
  • Lot #s 200910 and 200911, Exp 10/16
Distribution area
Nationwide

nationwide and UK

United States, United Kingdom

Quantity affected5951 units
Recall initiationFDA report date: September 3, 2014
FDA recall numberF-2398-2014

Beyond the headline

The recall, in context

Beta Labs initiated this food recall on June 20, 2013. The FDA enforcement report states: The products contain DMAA, also known as 1, 3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements. The FDA report lists distribution as: nationwide and UK.

The FDA enforcement report describes the reason as: The products contain DMAA, also known as 1, 3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.

Oxyphen Xr, 12 Hr / Clinical Strength Fat Burner, 45 Fast Acting Extended Release Capsules, … was made or distributed by Beta Labs in Memphis, TN, United States. This page reflects FDA report F-2398-2014, dated September 3, 2014.

Why this is a Class II recall

Class II means the product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the UPC and lot code against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Oxyphen Xr, 12 Hr / Clinical Strength Fat Burner, 45 Fast Acting Extended Release Capsules, … recall?

Beta Labs recalled Oxyphen Xr, 12 Hr / Clinical Strength Fat Burner, 45 Fast Acting Extended Release Capsules, … in an FDA Class II enforcement action reported as F-2398-2014. The products contain DMAA, also known as 1, 3-dimethylamylamine, methylhexamine or geranium extract, which is not permitted in dietary supplements.

What should I do if I bought this product?

Check the identifying codes below and stop using the product. Return it to the retailer for a refund or dispose of it safely, following the recall notice. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Beta Labs recall still active?

The FDA lists this recall as recall closed. It remains relevant if you still have the affected product or need to identify a historical recall.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record F-2398-2014. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Brand history

More recalls by Beta Labs

View brand
Class I·

Beta Labs

Phentalene (Tm), Pharmaceutical Grade, with 50 mg of Ephedra Extract, 90 Capsules, Distributed…

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

Nationwide (US) +1 countriesFood
Class II·

Beta Labs

Phenfx (Tm), Pheno 550 mg, Pharmaceutical Grade, 90 Capsules, Manufactured for: Beta Labs, LTD, …

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

Nationwide (US) +1 countriesFood

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Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.