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Class IOngoing

ZMB Enterprises recalls Addall XR Shot 1 single bottle

Recall date · record updated Sep 2, 2026 · Source: U.S. Food and Drug Administration (openFDA food enforcement)

What to do

Check your product against the names and codes above. The FDA enforcement record lists the recall as voluntary: firm initiated; it does not state a consumer remedy, so follow the firm’s notice or the FDA link.

Company
ZMB Enterprises
Reason
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
Hazard
FDA Class I: a reasonable probability that use or exposure will cause serious adverse health consequences or death (FDA definition).
Who’s affected
The firm markets their products online via their website addallxr.com
Official notice
www.accessdata.fda.gov/scripts/ires/index.cfm?Event=98691…

Products

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

    Codes/lots: Sold between July - December 2025Quantity: unknownRecall no. H-1263-2026Class I

Update history

  1. First listed on OVERLOOKED from the official record.

When the agency expands or changes this recall, we update this page and log the change here.

Proof: raw official record (JSON) · fetched from FDA API

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