Eyedrops maker couldn't ensure factory was sterile, FDA says

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Eyedrops maker couldn't ensure factory was sterile, FDA says
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The Food and Drug Administration says it found a host of problems at an Indian manufacturing plant recently linked to contaminated eyedrops.

is considered particularly worrisome because the bacteria driving it is resistant to standard antibiotics.

The report has the agency’s preliminary findings and is likely to be followed by a formal report and a warning letter to the company. An FDA spokesman said the inspection indicates that the company’s products “may be in violation of FDA’s requirements.” The FDA is responsible for assuring the safety of foreign products shipped to the U.S., though it has long struggled to keep pace with international pharmaceutical supply chains that increasingly begin in India and China.

Global Pharma has said little publicly about its recent recalls, instead referring questions to the U.S. companies that sold the products.

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