FDA recall H-1263-2026 · Sep 2, 2026
ZMB Enterprises: Addall XR Shot 1 single bottle recall
Product
Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
Reason for recall
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
What to do
FDA enforcement reports don't include consumer instructions. Check the codes below against your package, and look for the company's notice on FDA's recalls page. If you have the product and aren't sure, don't use it until you've checked.
Recall details
- FDA classification
- Class I: FDA's most serious class, where use of or exposure to the product may cause serious health problems or death.
- Status
- Ongoing
- Codes, lots and dates
- Sold between July - December 2025
- Quantity
- unknown
- Distribution
- The firm markets their products online via their website addallxr.com
- Recalling firm
- ZMB Enterprises, Carlsbad, CA
- Voluntary or mandated
- Voluntary: Firm initiated
- Recall started
- 2026-04-03
Source: openFDA enforcement record H-1263-2026 · search recall number H-1263-2026 in FDA's Enforcement Report.
Copied from the agency record without changes. Data as of Oct 14, 2026, 1:15 AM EDT. The agency notice is the final word.
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