HealthCare Industry Alerts

Arrow International, LLC, subsidiary of Teleflex, Inc Recalls Arrow AutoCAT 2, AC3 Intra-Aortic Balloon Pumps for Unexpectedly Short Battery Run Times

Dewei Medical Equipment Co. Recalls DNA/RNA Preservation Kits That Are Not Authorized, Cleared, or Approved by the FDA

Medtronic HeartWare Ventricular Assist Device (HVAD) System

ICS Medical Advisory (ICSMA-22-335-01) BD BodyGuard Pumps

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