ZMB Enterprises recall: Addall XR Shot 1 single bottle
ZMB Enterprises is recalling Addall XR Shot 1 single bottle. The U.S. Food and Drug Administration published the recall on September 2, 2026; it began on April 3, 2026. Distributed The firm markets their products online via their website addallxr.com.
Most serious Class I is the most serious level: a reasonable probability that using or eating the product will cause serious health problems or death.

Share
| Product | Addall XR Shot 1 single bottle |
| Brand | ZMB Enterprises |
| Type | Food |
| Classification | Class I |
| Recall date | April 3, 2026 |
| Published by FDA | September 2, 2026 |
| Recall ID | 98691 |
Recalled products
- Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
- FDA recall number
- H-1263-2026
- Codes, lots and dates
- Sold between July - December 2025
- Quantity
- unknown
- Classification
- Class I
Identifiers and details
- FDA event ID
- 98691
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Carlsbad, CA, United States
Why it was recalled
The reason the FDA lists: “The product contains 1,4-DMAA, Phenylethylamine and Phenibut.”
Where it was sold
Distribution as the FDA records it: “The firm markets their products online via their website addallxr.com”
What to do
Check the product name, size, lot code and dates against the list. Do not eat a recalled product, even if it looks and smells fine – throw it away or return it to the store for a refund, and clean surfaces it touched.
Official notice: FDA Enforcement Report record (event 98691, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
Other food recalls
| Date | Recall | Problem | Agency |
|---|---|---|---|
| Oct 7, 2026 | possible Salmonella contamination Most serious | FDA Class I | |
| Oct 7, 2026 | possible Salmonella contamination Most serious | FDA Class I | |
| Oct 7, 2026 | possible Salmonella and E. coli contamination Most serious | FDA Class I | |
| Oct 7, 2026 | undeclared shellfish Serious | FDA Class II | |
| Oct 7, 2026 | undeclared allergen ingredient Serious | FDA Class II | |
| Oct 7, 2026 | undeclared yellow Serious | FDA Class II |
About this recall
Is ZMB Enterprises Addall XR Shot 1 single bottle recalled?
Yes. ZMB Enterprises recalled it on April 3, 2026; FDA published it September 2, 2026 (Class I). Only the lots, dates or models listed on this page are included.
Why was it recalled?
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
What should I do if I have it?
Check the product name, size, lot code and dates against the list. Do not eat a recalled product, even if it looks and smells fine – throw it away or return it to the store for a refund, and clean surfaces it touched.
Where was it sold?
The firm markets their products online via their website addallxr.com.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.