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RECALL RECORD — CLASS IIIRecall closedF-0980-2013/FDA enforcement
Nbty INC.·Dietary Supplements·Dec 21, 2012

Met-rx Extreme Thermo Rage Watermelon Dietary Supplement, 8 FL

What you need to know

Class III

  • What happened

    Acetobacter lovaniensis was detected in a sample of the product tested by a private laboratory. This is an issue of commercial spoilage.

  • Health risk

    The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. 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 FDANationwide (US)More supplements

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Product identification

Source: FDA FOOD

Brand nameNbty INC.
Recalling firmNbty INC.Bohemia, NY, United States
UPC / barcodes
7 86560 50389 1
Lot / date codes
  • Lot # 430855, Expiration Date 12/21/12
  • Lot # 430856, Expiration Date 12/29/12
Distribution area
Nationwide

Nationwide and Puerto Rico

United States, Puerto Rico

Quantity affected40, 668 bottles (shipped and sold in cases of 12)
Recall initiationFDA report date: February 13, 2013
FDA recall numberF-0980-2013

Beyond the headline

The recall, in context

Nbty INC. initiated this supplements recall on December 21, 2012. The FDA enforcement report states: Acetobacter lovaniensis was detected in a sample of the product tested by a private laboratory. This is an issue of commercial spoilage. The FDA report lists distribution as: Nationwide and Puerto Rico.

The FDA enforcement report describes the reason as: Acetobacter lovaniensis was detected in a sample of the product tested by a private laboratory. This is an issue of commercial spoilage.

Met-rx Extreme Thermo Rage Watermelon Dietary Supplement, 8 FL was made or distributed by Nbty INC. in Bohemia, NY, United States. This page reflects FDA report F-0980-2013, dated February 13, 2013.

Why this is a Class III recall

Class III means the product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations. In this recall, a safety issue that does not fit the standard pathogen, allergen, chemical or quality categories.

FDA definition

The product is unlikely to cause adverse health consequences. These recalls are often related to labeling or quality violations.

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 Met-rx Extreme Thermo Rage Watermelon Dietary Supplement, 8 FL recall?

Nbty INC. recalled Met-rx Extreme Thermo Rage Watermelon Dietary Supplement, 8 FL in an FDA Class III enforcement action reported as F-0980-2013. Acetobacter lovaniensis was detected in a sample of the product tested by a private laboratory. This is an issue of commercial spoilage.

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 Nbty INC. 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-0980-2013. 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

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