Class IDietary supplement
Addall XR Shot 1 single bottle recall
Summary
ZMB Enterprises is recalling Addall XR Shot 1 single bottle (dietary supplement). According to the FDA report, the reason is: The product contains 1,4-DMAA, Phenylethylamine and Phenibut. The FDA rated this a Class I: most serious: there is a reasonable chance the product could cause serious health problems or death. Recall status: Ongoing.
Understanding this recall
What happened
ZMB Enterprises is recalling Addall XR Shot, a 2 oz liquid dietary supplement, because it contains 1,4-DMAA, phenylethylamine and phenibut.
Why it matters
Products sold as supplements or herbal remedies sometimes contain hidden drug ingredients or unapproved stimulants. People taking them can't know what dose they're getting, the ingredients can interact with other medicines, and stimulants such as DMAA have been linked to raised blood pressure and heart problems. The FDA has repeatedly warned consumers about hidden ingredients in these kinds of products. Phenibut isn't an approved drug in the U.S., and the FDA has said that DMAA isn't a lawful dietary ingredient.
Who should pay attention
Anyone who bought Addall XR online from the company's website.
Distribution in the FDA report: The firm markets their products online via their website addallxr.com
How to check your product
The report covers product sold between July and December 2025.
Codes listed by the FDA: Sold between July - December 2025
Based only on the FDA enforcement record plus general public-health background on this type of hazard. Not medical advice; if you have symptoms or concerns, contact a doctor or pharmacist.
Details from the FDA report
- Product
- Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- Reason
- The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
- Lot / code info
- Sold between July - December 2025
- Quantity
- unknown
- Distribution
- The firm markets their products online via their website addallxr.com
- Recalling company
- ZMB Enterprises, Carlsbad, CA United States
- Recall started
- April 3, 2026
- FDA report date
- September 2, 2026
- Classification
- Class I: Most serious: there is a reasonable chance the product could cause serious health problems or death.
- Voluntary / mandated
- Voluntary: Firm initiated
- Status
- Ongoing
- Recall number
- H-1263-2026
What to do
- Check whether you have this product, and compare the lot numbers, codes, or dates on your package with the codes listed above.
- If it matches, stop using it and keep it away from children and pets.
- Contact the recalling company (ZMB Enterprises) or the store where you bought it about returns or refunds.
- If you think the product made you or someone else sick, contact a doctor or pharmacist. In an emergency call 911.
- You can report problems to the FDA via MedWatch.