VerifyRecall
Alerts
ACTIVE RECALL — CLASS IActive recallH-1263-2026/FDA enforcement
Zmb Enterprises·Dietary Supplements·Apr 3, 2026

Addall Xr Shot 1 Single Bottle, 2 FL

What you need to know

Class I

  • What happened

    The product contains 1, 4-DMAA, Phenylethylamine and Phenibut.

  • Health risk

    The product has a reasonable probability of causing serious adverse health consequences or death. An unlabeled prescription or controlled substance was found in a product sold as food or a supplement.

  • Action required

    Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure.

Active recall · classified by the FDADistribution not listedMore supplements

Advertisement

Ad

Know someone who bought this?

A quick share can keep a pantry check from becoming a missed warning.

Share via WhatsApp

Match before you discard

Product identification

Source: FDA FOOD

Brand nameZmb Enterprises
Recalling firmZmb EnterprisesCarlsbad, CA, United States
UPC / barcodesNo UPC listed in the FDA enforcement record.
Lot / date codes
  • Sold between July - December 2025
Distribution area

The firm markets their products online via their website addallxr.com

United States

Quantity affectedNot provided by the FDA.
Recall initiationFDA report date: September 2, 2026
FDA recall numberH-1263-2026

Beyond the headline

The recall, in context

Zmb Enterprises initiated this supplements recall on April 3, 2026. The FDA enforcement report states: The product contains 1, 4-DMAA, Phenylethylamine and Phenibut. The FDA report lists distribution as: The firm markets their products online via their website addallxr.com.

The FDA enforcement report describes the reason as: The product contains 1, 4-DMAA, Phenylethylamine and Phenibut.

Addall Xr Shot 1 Single Bottle, 2 FL was made or distributed by Zmb Enterprises in Carlsbad, CA, United States. This page reflects FDA report H-1263-2026, dated September 2, 2026.

Why this is a Class I recall

Class I means the product has a reasonable probability of causing serious adverse health consequences or death. In this recall, an unlabeled prescription or controlled substance was found in a product sold as food or a supplement.

FDA definition

The product has a reasonable probability of causing serious adverse health consequences or death.

What to do now

  1. 1

    Stop using it

    Do not eat, drink or take the affected product.

  2. 2

    Check the codes

    Compare the lot and date codes against the table above.

  3. 3

    Return or discard

    Contact the retailer or recalling firm about a refund, and dispose of the product safely.

Consumer safety guide

Product safety recall

Symptoms to watch for

The official enforcement report describes the specific risk. Follow the recall notice, check the product codes and do not use a product that may be affected.

Higher-risk groups

Children, pregnant people, older adults and people with weakened immune systems should take extra care when a product's safety is uncertain.

What to do now

  1. 1Stop using or eating the product and keep it away from children and pets.
  2. 2Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return.
  3. 3Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Read the official source record for the specific hazard and instructions.

This is general consumer safety information, not medical advice or a diagnosis. Follow the official recall notice and contact a healthcare professional if you have concerns about exposure or symptoms.

Frequently asked

Questions about this recall

What is the Addall Xr Shot 1 Single Bottle, 2 FL recall?

Zmb Enterprises recalled Addall Xr Shot 1 Single Bottle, 2 FL in an FDA Class I enforcement action reported as H-1263-2026. The product contains 1, 4-DMAA, Phenylethylamine and Phenibut.

What should I do if I bought this product?

Stop taking the supplement. Check the lot and UPC codes below, then return it to the retailer or contact the manufacturer about a refund. Seek medical advice if you have concerns about exposure. Stop using or eating the product and keep it away from children and pets. Check the UPC and lot/date codes on this page and follow the official recall notice for disposal or return. Seek medical advice if anyone develops severe or worrying symptoms after exposure.

Is the Zmb Enterprises recall still active?

Yes. As of the latest FDA enforcement report, this recall is listed as ongoing. Check the official source record for the most current status before making a decision.

Where can I verify this recall?

This page is normalized from the openFDA enforcement record H-1263-2026. You can verify it directly using the official source link on this page. VerifyRecall updates its index from public FDA enforcement data and does not replace advice from the FDA, the recalling firm or a healthcare professional.

Verify before you act.

VerifyRecall is independent and not affiliated with the FDA. Always confirm the latest status on the official source record.

Official source

Related alerts

Recent Undeclared drug ingredient recalls

All alerts
Class I·

Jxk Enterprises, INC.

Boner Bears Chocolate, 3 Doses Per Bar, NET WT

JXK Enterprises, Inc is voluntarily recalling Boner Bears Chocolate, Lot #BB21125, after being notified that FDA laboratory analysis confirmed the presence of sildenafil, an…

Nationwide (US)Food
Class II·

Pacific Health Sciences LLC

Babies' Magic Tea

Adulterated (elevated levels of alcohol) infant dietary supplement

INSupplements

Record last synced from official openFDA enforcement data on November 14, 2026. Source record: official FDA notice.