Recall archive / 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. Source coverage and dates.
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
What the recall classes mean. 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.