The FDA and CDC found bacteria in three batches of preservative-free betamethasone and in a single batch of cardioplegia solution. The test results reinforce the lack of sterility in products manufactured by NECC and that healthcare providers should not use any of its products.
More Articles on Anesthesia:
All Ameridose Products Recalled as Sterility Precaution
Children Less Stressed Before Anesthesia Induction After Watching Videos
Report on Compounding Pharmacies by Congressman Shows Regulations Gaps
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