Addall XR Shot recall (September 2026): reason, lots, what to do
Not medical advice. This page reproduces one FDA enforcement report and explains its fields; FDA’s text is quoted as FDA’s. If you have this product and any symptoms, your pharmacist or doctor comes before this page.
What was recalled
ZMB Enterprises (Carlsbad, CA) recalled Addall XR Shot in a recall FDA classified as Class I. FDA’s stated reason: “The product contains 1,4-DMAA, Phenylethylamine and Phenibut.”. Started April 3, 2026; posted in the enforcement report September 2, 2026; status Ongoing.
Class I means, in FDA’s words, a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. Distribution: “The firm markets their products online via their website addallxr.com”. Quantity: unknown. Check your lot →
The FDA record
Everything in this table is copied from FDA’s enforcement report for event 98691, retrieved from openFDA on September 21, 2026; the last row links to the live record so you can confirm it has not changed.
| Recalling firm | ZMB Enterprises, Carlsbad, CA |
|---|---|
| Product | Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement |
| Reason for recall (FDA’s text) | “The product contains 1,4-DMAA, Phenylethylamine and Phenibut.” |
| Classification | Class I |
| Status | Ongoing |
| Recall type | Voluntary: Firm initiated |
| Recall initiated | 2026-04-03 |
| Enforcement report date | 2026-09-02 |
| FDA classified on | 2026-08-24 |
| Distribution | The firm markets their products online via their website addallxr.com |
| Quantity | unknown |
| How the firm notified | Press Release |
| Recall number | H-1263-2026 |
Lots, codes and how to check your bottle
FDA’s “code info” field for this event, verbatim:
Sold between July - December 2025
Find the lot number on the bottom of the container, beside the seal or on the box flap; the expiration date is usually printed next to it. If the code on your container appears above, it is in scope. If the product name matches but the code does not, your unit is not part of this recall, though a second lot is sometimes added later, so re-check the recall list before finishing the bottle.
Why this is a Class I recall
FDA assigns the class by the probability and severity of harm, not by how much product is involved. For this event the reason falls into what we file as hidden drug or prohibited ingredient: a substance that is not a lawful dietary ingredient was found in, or substituted for, the product. This is the recall category with the least warning for the buyer: the label reads like a supplement and the effect comes from something else.
FDA’s definition of Class I (21 CFR 7.3) is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death. A Class I recall is the strongest signal FDA sends about a consumer product short of a seizure; it is reserved for the cases where continuing to use the product is itself the risk. The reason text is the authority for this specific event; the class is FDA’s summary judgement of it.
If you bought it
- Stop taking it now; for a Class I recall this is the point of the notice.
- Match your lot against the codes above. Keep the container: the firm’s notice normally offers a refund on proof of the lot number or a photo.
- If you take prescription medicines, tell your pharmacist which product you were taking; an undeclared ingredient can interact with what you are prescribed. Then report to FDA MedWatch (online form or 1-800-FDA-1088).
- Check the firm’s other products. A recall event often expands to the same firm’s other SKUs a week or two later. Search “ZMB Enterprises” on the full recall list.
Choosing a replacement that can be checked
This product does not name an ingredient we track, so there is no like-for-like guide to send you to. The general rule holds: the only supplements whose contents a buyer can verify are those in a certifier’s public registry (NSF/ANSI 173, NSF Certified for Sport, USP Verified, Informed Sport) or with a lot-specific certificate of analysis the brand publishes. Our registry audit shows how few products clear that bar, and the per-ingredient third-party-tested pages (magnesium, creatine, vitamin D, omega-3, multivitamins) list the ones that do.
Frequently asked questions
Why was Addall XR Shot recalled?
FDA's enforcement report gives the reason as: "The product contains 1,4-DMAA, Phenylethylamine and Phenibut.". FDA records the recall type as "Voluntary: Firm initiated"; ZMB Enterprises of Carlsbad, CA started it April 3, 2026 and it was posted in FDA's enforcement report on September 2, 2026 as Class I.
Which lots of Addall XR Shot are affected?
FDA's record lists: Sold between July - December 2025. Match these against the lot number, UPC or expiration date printed on your container; a bottle whose code is not listed is not part of this recall.
Where was Addall XR Shot sold?
FDA's record gives the distribution as: "The firm markets their products online via their website addallxr.com". Quantity recalled: unknown.
Is this recall over?
FDA lists the status as "Ongoing". Ongoing means the firm is still retrieving product from the market.
← Every FDA dietary supplement recall since 2023 · How we score supplement safety
Sources
- U.S. Food and Drug Administration. Enforcement report, event 98691, recall number H-1263-2026. Via openFDA Food Enforcement API, retrieved September 21, 2026. H-1263-2026
- 21 CFR 7.3(m): recall classification definitions. eCFR Title 21 Part 7.
- FDA. MedWatch: The FDA Safety Information and Adverse Event Reporting Program. fda.gov/safety/medwatch.