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Fungal Meningitis Archives

Ameridose Issues Recall of All Products

October 31, 2012
 Dear Customer:
 Ameridose is conducting a voluntary recall of any unexpired products remaining in circulation. This action is voluntary, and represents an expansion of our cooperation with the U.S. Food and Drug Administration and the Massachusetts Board of Registration in Pharmacy.
During the course of its on-going inspection of our facility, FDA has notified Ameridose that it will be seeking improvements in Ameridose's sterility testing process. 

CDC Responds to Multistate Meningitis Outbreak

The Centers for Disease Control and Prevention (CDC) and the  Food and Drug Administration (FDA) are currently coordinating a multistate  investigation of fungal infection among patients who received a steroid  injection with a potentially contaminated product either into the spinal area or  in a joint space, such as a knee, shoulder or ankle.

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Goethel Engelhardt, PLLC
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Ann Arbor, MI 48103

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