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RECALL RECORD — CLASS IRecall closedF-1371-2014/FDA enforcement
Usplabs, LLC·Dietary Supplements·Nov 9, 2013

Usplabs Oxyelite Pro Ultra-intense Thermo Advanced Formula Dietary Supplement Manufactured For…

What you need to know

Class I

  • What happened

    USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with…

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. A safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Recall closed · classified by the FDADistribution not listedMore supplements

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Product identification

Source: FDA FOOD

Brand nameUsplabs, LLC
Recalling firmUsplabs, LLCDallas, TX, United States
UPC / barcodes
0 94922 44788 30 94922 44787 60 94922 39562 70 94922 44786 9
Lot / date codes
  • 3 count capsules, UPC #094922447883
  • 3 count capsules UPC #094922447876
  • 90 count capsules, UPC #094922395627
  • 180 count capsules UPC #094922447869
Distribution area

Worldwide distribution including the following Worldwide distribution including the following international countries: Ecuador, Russia, UAE, South America, Dominican Republic, Kuwait, Philippines, Indonesia, Egypt, Panama, China, and Argentina.

China

Quantity affected1, 065, 783 units
Recall initiationFDA report date: January 22, 2014
FDA recall numberF-1371-2014

Beyond the headline

The recall, in context

Usplabs, LLC initiated this supplements recall on November 9, 2013. The FDA enforcement report states: USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse health events, namely serious liver damage or acute liver failure. The FDA report lists distribution as: Worldwide distribution including the following Worldwide distribution including the following international countries: Ecuador, Russia, UAE, South America, Dominican Republic, Kuwait, Philippines, Indonesia, Egypt, Panama, China, and Argentina.

The FDA enforcement report describes the reason as: USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with serious adverse health events, namely serious liver damage or acute liver failure.

Usplabs Oxyelite Pro Ultra-intense Thermo Advanced Formula Dietary Supplement Manufactured For… was made or distributed by Usplabs, LLC in Dallas, TX, United States. This page reflects FDA report F-1371-2014, dated January 22, 2014.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

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 Usplabs Oxyelite Pro Ultra-intense Thermo Advanced Formula Dietary Supplement Manufactured For… recall?

Usplabs, LLC recalled Usplabs Oxyelite Pro Ultra-intense Thermo Advanced Formula Dietary Supplement Manufactured For… in an FDA Class I enforcement action reported as F-1371-2014. USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with…

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. 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 Usplabs, LLC 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-1371-2014. 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 Usplabs, LLC

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Usplabs, LLC

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USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with…

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Class I·

Usplabs, LLC

Usplabs Oxyelite Pro Super Thermo Dietary Supplement Manufactured for Usplabs, LLC (Dallas, Tx…

USPlabs, LLC received a 423(a), Notification of Opportunity to Initiate a Voluntary Recall, letter from FDA and is recalling products containing Aegeline and associated with…

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