← FDA ENFORCEMENT
H-1263-2026Class I
ZMB Enterprises
What this record is not
A recall record is reproduced as FDA published it, and the classification is FDA’s. SPEQ adds no interpretation, and a recall concerns the products and dates in the record — it is not a statement about a company’s other products or its current status.
Recalling firm
ZMB Enterprises
Product type
Food / supplement / cosmetic
Status
Ongoing
Report date
2026-09-02
Distribution
The firm markets their products online via their website addallxr.com
Firm state
CA
Product quantity
unknown
Initiated by
Voluntary: Firm initiated
Reason for recall
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
Product description
Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
Code / lot info
Sold between July - December 2025
Data: U.S. FDA. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification. Open the enforcement explorer →