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NEWS FLASH
06/18/2021
FDA Recall - Infusion Pump Repair - Alaris Bezel
We are writing to inform you that effective immediately the FDA has issued notice of a Class 1 recall of the Alaris Infusion Pump Module Model 8100 Bezel, Product Number TIPA-8100-4410, Lot number 20200608 distributed from January 15, 2021 to March 14, 2021 that where purc..
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06/18/2021
FDA Recall - Phillips Sleep and Resp Care Devices
We are writing to inform you that effective immediately the FDA has issued notice of a voluntarynationwide recall by Philips for specific Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices to addr..
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06/15/2021
Notice of Prior Authorization Requirements
To provide information on CareCentrix's prior authorization requirements and changes to those requirements...
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