Laboratory samples from two additional recalled products from the New England Compounding Center have tested positive for bacterial contamination, according to the American Society of Anesthesiologists.
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.
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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:
Dicolfenac Provides Significant Pain Relief for Abdominal, Pelvic Surgeries
Can ASCs Still Profit From Anesthesia? A Review of OIG Guidance
Anesthesiologist Dr. Brian Waltmann Joins MedNet as Medical Director