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FDA recall 98691: ZMB Enterprises: Addall XR Shot 1 single bottle

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FDARecall 98691Food

What to do

The FDA record of this recall has no instruction for consumers. Compare the lot codes below with your product. If they match, do not use it, and follow the notice of the firm or ask the store where you bought it. Note from Recalls Watch, not agency text.

Read the official notice on accessdata.fda.gov (opens in a new tab)

Hazard

Why it was recalled

The product contains 1,4-DMAA, Phenylethylamine and Phenibut.
Text from FDA, unedited.

FDA classification: Class I. FDA’s highest class: a reasonable probability that using the product will cause serious health consequences or death. Status: Ongoing.

Is it yours? Products and codes

  • Addall XR Shot 1 single bottle, 2 fl. oz., liquid dietary supplement

    Lot or code
    Sold between July - December 2025
    FDA recall number
    H-1263-2026
    Quantity
    unknown

Distribution (FDA): The firm markets their products online via their website addallxr.com

About this record

Issued by
U.S. Food and Drug Administration
Firm
ZMB Enterprises
Title
Composed by Recalls Watch from fields of the record; FDA records have no title.

If someone was hurt or swallowed something: call 911, or Poison Help at 1-800-222-1222.

About this recall

What is the hazard?

FDA states: “The product contains 1,4-DMAA, Phenylethylamine and Phenibut.”

What should I do if I have this product?

The FDA record of this recall has no instruction for consumers. Compare the lot codes on the notice with your product and follow the notice of the firm. The official report is linked on this page.

How do I know if my product is included?

Compare the lot or code printed on your product with the codes FDA lists on this notice, product by product.

When was this recall published?

FDA published recall 98691 on September 2, 2026.

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