The Food and Drug Administration (FDA) is alerting health care professionals and patients not to use drug products produced by Cantrell Drug Company of Little Rock, Arkansas, including opioids and other drugs intended for sterile injection, because there are serious deficiencies with the company’s compounding operations that put the sterility of the products into question. The FDA cautioned in a news release that administration of contaminated or otherwise poor quality drug products can result in “serious and life-threatening injury or death.” “A key aspect of the FDA’s mission to protect public health is creating a regulatory framework that helps ensure ... Read More
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