Prolatis’ Issues a Voluntary Nationwide Recall of its product ...

Courtesy Food and Drug Administration--Recalls  Thu, 08/12/2010 - 16:44

Salt Lake City, UT announced today that it is conducting a voluntary nationwide recall of the company’s product sold under the name Prolatis’.

Prolatis’ is conducting a voluntary recall after being informed by the Food and Drug Administration (FDA) that lab analysis has found Prolatis’ to contain Sulfoaildenafil, an analogue of Sildenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED), making Prolatis’ an unapproved drug.

The active drug ingredient is not listed on the product label. Product...


 

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