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Changes To Prior Authorization Requirements
To provide information on CareCentrix┬┐s prior authorization requirements and changes to those requirements...
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FDA Recall - BD Alaris PC Unit
To inform providers that that effective immediately the FDA has issued a Class I recall of BD CareFusion 303, Inc.┬┐s Alaris System PC unit and PC unit front case keypad replacement kits manufactured from April 7, 2017 to June 15, 2020 and distributed from April 12, 2017 to..
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FDA Recall - BD Alaris Pumps Recall
We are writing to inform you that effective immediately the FDA has announced a Class I recall as an update to their previously announced voluntary recall on June 30, 2020 of BD Alaris System Hardware. The hardware issues may cause the infusion pump to not operate as expec..
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