FDA recall, , High risk
ZMB Enterprises Addall XR Shot Dietary Supplement
Addall XR Shot contains 1,4-Dmaa, Phenylethylamine and Phenibut.
Summary by Recall Canary from the FDA notice
What happened
ZMB Enterprises of Carlsbad, California recalled Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement because it contains 1,4-DMAA, Phenylethylamine and Phenibut. The recall began April 3, 2026, and was added to the FDA's Enforcement Report on August 24, 2026. The firm markets the product online via its website addallxr.com.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for food recalls:
- Return it to the store where you bought it, or throw it away.
- Don't give it to anyone else, such as a food bank, or to a pet.
Is your bottle affected?
Compare these details with yours, then check the recall notice to see which units are recalled.
Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- Affected units
- Sold between July - December 2025
Recall details
- Company began the recall
- Sold in
The firm markets their products online via their website addallxr.com
- Company
- ZMB EnterprisesCarlsbad, California
- Hazard
- Hidden drug ingredient
- Risk
High risk
There is a reasonable chance that eating it could cause serious health problems or death.
FDA Class I recall · How risk is rated
- Event ID
- 98691
- Recall number
- H-1263-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
In FDA's weekly enforcement report
Listed on Recall Canary
Summary updated
