Recall map → All recalls → H-1263-2026
Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement ZMB Enterprises · reported 2026-09-02
Ongoing The agency has not recorded this recall as closed out.
- Reason for recall
- The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
- Classification
- Class I
- Recall initiated
- 2026-04-03
- Reported by the agency
- 2026-09-02
- Closed out (terminated)
- not reported
- Recalling firm
- ZMB Enterprises
Carlsbad, CA
United StatesThis is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.
- Distribution (the agency's own words)
- The firm markets their products online via their website addallxr.com
- States we parsed from that text
- could not be parsed
No state list could be read from the agency's text. Absence here is not evidence the product stayed put.
- Food category
- Dietary supplementsderived
Assigned by a reviewed keyword rulebook over the product description, not by the agency.
- Recall type
- Voluntary: Firm initiated
- Recall number
- H-1263-2026
Verifying this record. Everything above is FDA's own record, reproduced. FDA publishes no web page for an individual enforcement report, so the only direct link is the machine-readable one:
Open the raw FDA record (JSON) →
To look it up yourself, search recall number H-1263-2026 in FDA's Enforcement Report. That search cannot be linked to directly, so the number has to be pasted in.
This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.