FDA Drug Recalls

Recalls / Class I

Class ID-1376-2014

Class I— FDA's most serious classification, issued when there is a reasonable probability that use of or exposure to the drug will cause serious adverse health consequences or death.

Product

SlimEasy Herbs Capsule, 400 mg, supplied in 30 count boxes, distributed by MyNicKnaxs, LLC, Deltona, FL

Affected lot / code info
ALL LOTS

Why it was recalled

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

Recalling firm

Firm
MyNicNaxs, Inc.
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
1012 Alpine Dr, N/A, Deltona, Florida 32725-7204

Distribution

Quantity
2 boxes
Distribution pattern
Nationwide

Timeline

Recall initiated
2014-01-24
FDA classified
2014-06-12
Posted by FDA
2014-06-18
Terminated
2019-10-02
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-1376-2014. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class I recall: drug · FDA Drug Recalls