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ACTIVE RECALL — CLASS IIActive recallH-0168-2027/FDA enforcement
Pacific Health Sciences LLC·Dietary Supplements·Oct 6, 2026

Babies' Magic Tea

What you need to know

Class II

  • What happened

    Adulterated (elevated levels of alcohol) infant dietary supplement

  • Health risk

    The product may cause temporary or medically reversible health consequences, or the probability of serious harm is remote. An alcohol level that exceeds the product's label or an acceptable limit, particularly concerning in products for infants.

  • 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.

Active recall · classified by the FDAINMore supplements

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Match before you discard

Product identification

Source: FDA FOOD

Brand namePacific Health Sciences LLC
Recalling firmPacific Health Sciences LLCOxnard, CA, United States
UPC / barcodes
8 50302 00818 3
Lot / date codes
  • Lot: 25122bw Expiration date: 12/2028
Distribution area
IN

Product was manufactured for a single customer located in Florida. Product was made available through Amazon and through the customers website.

United States

Quantity affected953 units
Recall initiationFDA report date: October 28, 2026
FDA recall numberH-0168-2027

Beyond the headline

The recall, in context

Pacific Health Sciences LLC initiated this supplements recall on October 6, 2026. The FDA enforcement report states: Adulterated (elevated levels of alcohol) infant dietary supplement. The FDA report lists distribution as: Product was manufactured for a single customer located in Florida. Product was made available through Amazon and through the customers website.

The FDA enforcement report describes the reason as: Adulterated (elevated levels of alcohol) infant dietary supplement

Babies' Magic Tea was made or distributed by Pacific Health Sciences LLC in Oxnard, CA, United States. This page reflects FDA report H-0168-2027, dated October 28, 2026.

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, an unlabeled prescription or controlled substance was found in a product sold as food or a supplement.

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 Babies' Magic Tea recall?

Pacific Health Sciences LLC recalled Babies' Magic Tea in an FDA Class II enforcement action reported as H-0168-2027. Adulterated (elevated levels of alcohol) infant dietary supplement

What are the symptoms of Product safety recall exposure?

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.

Who is most at risk from Product safety recall?

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

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.

How do I get a refund from Pacific Health Sciences LLC?

Contact the recalling company or the retailer where you purchased the product, quote the FDA recall number and ask about a refund or replacement. Keep the packaging, lot code and proof of purchase where possible. The FDA does not issue consumer refunds. Reference FDA recall H-0168-2027 and keep the packaging, lot code and proof of purchase if you have them.

Is the Pacific Health Sciences LLC recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-0168-2027. 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.