Addall XR Shot recall
Recalled by ZMB Enterprises
The product, as the FDA describes it: Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
Why it was recalled
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
What to do if you have it
The agency has published the reason above without naming a health hazard class of its own. Match your package against the codes below, and when it matches, return it rather than deciding for yourself whether it looks fine.
How to tell whether your package is one of them
A recall covers particular production runs, not everything the company makes, so the codes decide it. These are the ones the FDA published. Match them against what is printed on your package, usually near the best-before date.
Sold between July - December 2025
The details on record
| Recalling company | ZMB Enterprises |
|---|---|
| Company location | Carlsbad, CA |
| Where it was distributed | The firm markets their products online via their website addallxr.com |
| How much was recalled | unknown |
| Recall started | April 3, 2026 |
| Published by the FDA | September 2, 2026 |
| Recall type | Voluntary: Firm initiated |
| How the company announced it | Press Release |
| FDA recall number | H-1263-2026 |
Everything above comes from the FDA enforcement report for this recall. Read the official notice for the company's own wording, contact numbers, and any photographs of the packaging.
The other half of the answer
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