ZMB Enterprises food recall: Addall XR Shot 1 single bottle
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Ongoing
- Event ID
- 98691
- Recall initiated
- Apr 3, 2026
- Classified by FDA
- Aug 24, 2026
- Posted in Enforcement Report
- Sep 2, 2026
- Recalling firm
- ZMB Enterprises
- Firm location
- Carlsbad, CA, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Press Release
- Products in this event
- 1
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Apr 3, 2026. FDA classified it 143 days later, on Aug 24, 2026. Distribution reported by FDA: The firm markets their products online via their website addallxr.com
Recalled products (1)
H-1263-2026 Class I Ongoing
Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
Codes / lots: Sold between July - December 2025
Quantity: unknown
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 98691
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.