CLASS I ONGOING Food recall · Reported 2 Sep 2026 · FDA Enforcement Report
Addall XR Shot, liquid dietary supplement recalled by ZMB Enterprises
ZMB Enterprises is recalling Addall XR Shot, liquid dietary supplement. The recall was initiated on 3 Apr 2026 and the FDA has classified it as Class I.
Check your package
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
Recall details
- Recall number
- H-1263-2026
- FDA event ID
- 98691
- Recalling firm
- ZMB Enterprises, Carlsbad, CA
- Brand
- Addall XR
- Classification
- Class I
- Status
- Ongoing
- Recall initiated
- 3 Apr 2026
- FDA classified
- 24 Aug 2026
- Reported
- 2 Sep 2026
- Type
- Voluntary: Firm initiated
- Customers notified by
- Press Release
- Reason category
- Hidden Drug Ingredients
- Product category
- Dietary Supplements
Timeline
| 3 Apr 2026 | Recall initiated by company | |
| 24 Aug 2026 | Classified by FDA | +143 days |
| 2 Sep 2026 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.
Product as listed by the FDA
Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement
Where it was distributed
The firm markets their products online via their website addallxr.com
Stores named: Online Retailers
Questions about this recall
Why was it recalled?
The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
Which lots are affected?
Sold between July - December 2025
Where was it sold?
The firm markets their products online via their website addallxr.com
What should I do if I have it?
Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.
What does Class I mean?
Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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