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RECALL RECORD — CLASS IIRecall closedF-0646-2023/FDA enforcement
Ba Sports Nutrition, LLC·Food·Feb 28, 2023

Bodyarmor Sportwater 24/700ml

What you need to know

Class II

  • What happened

    Potential for plastic pieces in product

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. Plastic fragments can pose a choking risk or irritate and injure the digestive tract.

  • 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 FDAIL, KS, SD, OR +7 moreMore food

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Product identification

Source: FDA FOOD

Brand nameBa Sports Nutrition, LLC
Recalling firmBa Sports Nutrition, LLCWhitestone, NY, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • All codes up to and including BB 021624 UNX LO4
Distribution area
ILKSSDORWAMNUTALIATXAR

IL, KS, SD, OR, WA, MN, UT, AL, IA, TX, AR

United States

Quantity affectedapproximately 21, 000, 000 bottles
Recall initiationFDA report date: March 29, 2023
FDA recall numberF-0646-2023

Beyond the headline

The recall, in context

Ba Sports Nutrition, LLC initiated this food recall on February 28, 2023. The FDA enforcement report states: Potential for plastic pieces in product. The FDA report lists distribution as: IL, KS, SD, OR, WA, MN, UT, AL, IA, TX, AR.

The FDA enforcement report describes the reason as: Potential for plastic pieces in product

Bodyarmor Sportwater 24/700ml was made or distributed by Ba Sports Nutrition, LLC in Whitestone, NY, United States. This page reflects FDA report F-0646-2023, dated March 29, 2023.

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, plastic fragments can pose a choking risk or irritate and injure the digestive tract.

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 lot and date codes 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

Plastic contamination

Possible health effects

Plastic fragments can pose a choking risk or cause irritation or injury to the mouth and digestive tract.

Higher-risk groups

Young children and anyone who may swallow a fragment without noticing are at greater risk.

What to do now

  1. 1Stop eating or using the product and do not taste or chew it to check for fragments.
  2. 2Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting.
  3. 3Keep the packaging and contact the retailer or manufacturer about a refund.

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 Bodyarmor Sportwater 24/700ml recall?

Ba Sports Nutrition, LLC recalled Bodyarmor Sportwater 24/700ml in an FDA Class II enforcement action reported as F-0646-2023. Potential for plastic pieces in product

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 eating or using the product and do not taste or chew it to check for fragments. Seek medical care if anyone has swallowed plastic or has breathing difficulty, severe pain or persistent vomiting. Keep the packaging and contact the retailer or manufacturer about a refund.

Is the Ba Sports Nutrition, 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-0646-2023. 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

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