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FDA issues alert on Reumofan Plus

Health officials in Mexico order recall based on potentially harmful pharmaceutical ingredients in Reuofan Plus. The U.S. Food and Drug Administration is warning consumers that Reumofan Plus, marketed as a “natural� dietary supplement for pain relief and other serious conditions, contains several active pharmaceutical ingredients not listed on the label that could be harmful.

FDA warns consumers about counterfeit version of Teva’s Adderall

The U.S. Food and Drug Administration is warning consumers and health care professionals about a counterfeit version of Teva Pharmaceutical Industries’ Adderall 30 milligram tablets that is being purchased on the Internet. Adderall, which is approved to treat attention deficit hyperactivity disorders (ADHD) and narcolepsy, is a prescription drug classified as a controlled substance, a class of drugs for which special controls are required for dispensing by pharmacists.

FDA warns consumers about counterfeit version of Teva’s Adderall

The U.S. Food and Drug Administration is warning consumers and health care professionals about a counterfeit version of Teva Pharmaceutical Industries’ Adderall 30 milligram tablets that is being purchased on the Internet. Adderall, which is approved to treat attention deficit hyperactivity disorders (ADHD) and narcolepsy, is a prescription drug classified as a controlled substance – a class of drugs for which special controls are required for dispensing by pharmacists.

Urgent: Compounded Prescription Recall

This is to inform you of a product recall involving: All Sterile Human and Veterinary Prescriptions Distributed by Franck’s Pharmacy
From November 21, 2011 to May 21, 2012. This recall is being initiated after the U.S. Food and Drug Administration (“FDA”) notified us that environmental sampling of our clean room revealed the presence of microorganisms and fungal growth.