Food recall

ZMB Enterprises recall: Addall XR Shot 1 single bottle

ZMB Enterprises, of Carlsbad, CA, recalled Addall XR Shot 1 single bottle. The FDA's reason: “The product contains 1,4-DMAA, Phenylethylamine and Phenibut.” The FDA classified it Class I: it could cause serious harm or death. The company began the recall voluntarily on April 3, 2026, and the FDA first listed it in its Enforcement Report of September 2, 2026. The recall is still going on.

How serious

Class I

It could cause serious harm or death

Why

See FDA's words below

Status

Ongoing

The recall

Company
ZMB Enterprises (Carlsbad, CA)
Reason, in FDA's words
“The product contains 1,4-DMAA, Phenylethylamine and Phenibut.”
Where it was sold
The firm markets their products online via their website addallxr.com
Recall began
, by the company
FDA classified it
First in an FDA Enforcement Report
FDA event number
98691

The product recalled

As the FDA describes them, with the codes that tell whether a package is part of the recall.

  • H-1263-2026 Class I

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

    Codes: Sold between July - December 2025

    Quantity: unknown

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Source and notes

U.S. Food and Drug Administration, Enforcement Reports (openFDA food recall data) (Public domain (U.S. government work); source U.S. Food and Drug Administration, openFDA), data as of September 2, 2026.

Each week the FDA lists the recalls it has classified in its Enforcement Report, often weeks after the company announced the recall, so a month with five weekly reports tends to count more. Each recall counts once, however many products it covers, in the month FDA first listed it. Class I means the food could cause serious harm or death, Class II temporary or minor harm, and Class III is unlikely to harm anyone. Meat, poultry and most egg products are recalled by the U.S. Department of Agriculture, not the FDA, and aren't included. For what to do with a recalled product, see the FDA's recalls page.