A liquid supplement for infants sold in the United States via Amazon and other online marketplaces has been voluntarily pulled from shelves after the Food and Drug Administration (FDA) found undeclared ethanol, methanol, and isopropanol. The recall pertains solely to one specific batch of Babies' Magic Tea Baby Sleep Gripe Water, marketed as a remedy for digestive discomfort and to aid infant sleep.
Details of the Withdrawal
Pacific Health Sciences announced the recall on October 6, 2026, with the FDA releasing a public notice the following day. Tests on the affected batch revealed approximately 8.3% ethanol, 0.35% methanol, and 0.48% isopropanol, none of which were listed as ingredients on the product label.
The company highlighted the potential risk these substances pose depending on the amount consumed, alongside the age and weight of the infant. Although no adverse effects related to the batch have been reported, Pacific Health Sciences advises checking the packaging and discontinuing use if it matches the recalled product.
Identifying the Recalled Product
The recall is linked to the following details, as published by the FDA:
- Brand and Product: Babies' Magic Tea, Baby Sleep Gripe Water
- Batch Number: 25122bw
- Best Before Date: 12/2028
- Content: 4 fluid ounces (approximately 118 milliliters)
- Packaging: Amber bottle in a blue cardboard box, includes an oral syringe
- Batch Location: Bottom of the box and a side panel of the bottle
This warning does not constitute a general recall of all products from the brand. It is specifically related to batch 25122bw, making it crucial to verify the code before drawing any conclusions about other packages.
Distribution and Consumer Advice
The supplement was distributed to Secrets of Tea for sale through digital channels, including Amazon and the Secrets of Tea website. The announcement does not specify the number of units sold or provide a breakdown by state.
Families who purchased the product online should examine both the box and bottle, even if the purchase occurred weeks or months ago. The involvement of a retailer does not imply that it is the supplement's manufacturer.
Steps for Parents with Affected Product
Pacific Health Sciences, via the FDA, recommends immediately discontinuing use of any container from batch 25122bw and either disposing of it or returning it to the place of purchase for a refund. The product should not be administered to infants during the return process.
If a child has consumed the supplement and exhibits symptoms, the official notice advises seeking medical attention and contacting the company. In the United States, the Poison Help hotline provides free guidance at 1-800-222-1222, even before symptoms appear. In cases of respiratory distress, seizures, unconsciousness, or inability to wake the child, poison control centers recommend calling 911 immediately.
Experts also advise against inducing vomiting in the event of potential toxic ingestion; it is better to receive tailored advice from healthcare professionals, following Poison Control's first aid guidelines.
Contact Information for Inquiries
For questions about the recall or to report a possible reaction, Pacific Health Sciences can be reached at 310-457-1775 or myorder@pacifichealth.com, Monday through Thursday, from 9:30 a.m. to 5:00 p.m. Pacific Time. Adverse reactions can also be reported through the FDA's MedWatch system.
The Implication of Finding Three Alcohols in an Infant Supplement
The discovery includes ethanol, the alcohol found in alcoholic beverages; methanol, a toxic substance that can lead to severe poisoning if ingested; and isopropanol, an alcohol used in various industrial and cleaning products. These substances are not equivalent, and their effects depend on factors such as dosage and exposure circumstances.
In this instance, the FDA has not reported any confirmed poisonings linked to the batch nor explained how these compounds entered the product. As such, it should not be assumed that all children who consumed it have been harmed. The potential severity and absence of these components on the label warrant the recommendation to discontinue use.
Products marketed as dietary supplements do not undergo the same pre-approval process as medications. The FDA states in Spanish that the primary responsibility for ensuring product safety and correct labeling lies with manufacturers and distributors, with the agency stepping in when violations are detected.
This recent alert underscores the importance of paying attention to batch numbers and official recall notices, particularly for products intended for infants. Previously, CiberCuba reported on another recall involving products sold through Amazon and other US retailers, though that case pertained to deodorants and had a different cause.
FAQs About the Infant Supplement Recall
What should parents do if they have the recalled product?
Parents should immediately stop using the product from batch 25122bw, dispose of it, or return it to the purchase location for a refund. Do not administer it to the infant while arranging a return.
How can one identify the affected product batch?
The affected product is Babies' Magic Tea Baby Sleep Gripe Water from batch 25122bw, with a best before date of 12/2028. It comes in a 4-ounce amber bottle inside a blue box, with the batch number located on the bottom of the box and a side panel of the bottle.
What actions should be taken if a child shows symptoms after consuming the supplement?
Seek medical attention immediately and contact the company for guidance. For suspected poisoning, reach out to the Poison Help hotline at 1-800-222-1222 for free assistance, or call 911 in severe cases.