FDA Food · H-1263-2026

Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement

Class I · Ongoing

The product contains 1,4-DMAA, Phenylethylamine and Phenibut.

Affected lots / codes — check yours against thisSold between July - December 2025

Recalling firm: ZMB Enterprises, Carlsbad, CA
Classification: Class I (most serious — risk of serious harm)
Status: Ongoing
Quantity: unknown
Distribution: The firm markets their products online via their website addallxr.com
Recall initiated: April 3, 2026
Classified: August 24, 2026
Initiation: Voluntary: Firm initiated

Official source. This record is published by the U.S. FDA through the openFDA enforcement database. View the unmodified government record:
https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22

Important. Recalls target specific lots and codes — compare the affected lots above against your own product. This page reproduces public FDA data for readability; EveryRecall is independent and not affiliated with the FDA.

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