MyNicNaxs Meizitang Strong Version Botanical Slimming Recall

Why it was recalled

Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: N-desmethylsibutramine, benzylsibutramine, and sibutramine

Product description

Meizitang Strong Version Botanical Slimming, Soft Gel Capsules, 650 mg, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL

Lot numbers, UPCs & expiration codes

ALL LOTS

Where it was sold

Nationwide

What to do if you have this product

Compare the lot number and expiration date on your package with the codes above.
Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
If you have symptoms you think are related, contact your doctor. In an emergency call 911.
Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number: D-1380-2014
Classification: Class I
Status: Terminated
Recall initiated: Jan 24, 2014
FDA report date: Jun 18, 2014
Quantity: unknown
Recall type: Voluntary: Firm initiated
Recalling firm: MyNicNaxs, Inc.

Original FDA data

Every field from FDA enforcement report D-1380-2014, exactly as published.

Show all FDA fields

City: Deltona
State: FL
Status: Terminated
Country: United States
Event ID: 67471
Address: 1012 Alpine Dr
Code information: ALL LOTS
Postal code: 32725-7204
Report date: Jun 18, 2014
Product type: Drugs
Recall number: D-1380-2014
Classification: Class I
Recalling firm: MyNicNaxs, Inc.
Product quantity: unknown
Termination date: Oct 2, 2019
Reason for recall: Marketed Without an Approved NDA/ANDA: Product was found to contain undeclared active pharmaceutical ingredients: N-desmethylsibutramine, benzylsibutramine, and sibutramine
Voluntary / mandated: Voluntary: Firm initiated
Product description: Meizitang Strong Version Botanical Slimming, Soft Gel Capsules, 650 mg, supplied in 30 count bottles, distributed by MyNicKnaxs, LLC, Deltona, FL
Distribution pattern: Nationwide
Recall initiation date: Jan 24, 2014
Initial firm notification: E-Mail
Center classification date: Jun 12, 2014

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-1380-2014, published Jun 18, 2014. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: Oct 2, 2026. Content last changed: Oct 2, 2026.

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