FDA Drug Recalls

Recalls / Class I

Class ID-0961-2016

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

Thin and Slim Fataway Ultimate Stack with Chromium, packaged per 120 capsules. Distributed by Dale H Enterprises Inc. Lewisburg, PA 17837, www.fataway.org.

Affected lot / code info
UPC 853002003025

Why it was recalled

Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence of Salicylic acid in dietary supplements.

Recalling firm

Firm
Novacare, LLC
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
312 W 6100 S, N/A, Murray, Utah 84107-6990

Distribution

Quantity
N/A
Distribution pattern
Nationwide

Timeline

Recall initiated
2015-08-24
FDA classified
2016-06-06
Posted by FDA
2016-06-15
Terminated
2017-08-30
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0961-2016. 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