---
title: "Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement — FDA record H-1263-2026 | Is It on Recall"
description: "The product contains 1,4-DMAA, Phenylethylamine and Phenibut."
url: https://isitonrecall.com/recall/fda-food-h-1263-2026-addall-xr-shot-1-single-bottle-2-fl-oz-liquid-dietary-supplement/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA food enforcement

# Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement — FDA record H-1263-2026

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Apr 3, 2026. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- **Reason**: The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
- **Classification**: Class I
- **Recalling firm**: ZMB Enterprises
- **Quantity**: unknown
- **Agency-reported status**: Ongoing
- **Source record identifier**: H-1263-2026

[Open the official record](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | Sold between July - December 2025 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

The firm markets their products online via their website addallxr.com

No US distribution state could be established from this record. Check the official notice.

## Dates in the source

- **Report date**: Sep 2, 2026
- **Recall initiation date**: Apr 3, 2026
- **Center classification date**: Aug 24, 2026

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/food/enforcement.json?search=recall_number%3A%22H-1263-2026%22)

## Related records

[Supplements records](https://isitonrecall.com/product/supplements/) [Supplements records](https://isitonrecall.com/category/supplements/) [ZMB Enterprises records](https://isitonrecall.com/brand/zmb-enterprises/)