November 2017 – ESRD Network 10

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Diabetes Infusion Sets by Medtronic

Recall - Vent Membrane May be Susceptible to Being Blocked by Fluid See the FDA Safety Alert ISSUE: Medtronic is informing patients worldwide of a voluntary recall of specific lots of infusion sets used with all models of Medtronic insulin pumps. The recall is related to a certain discontinued component in these infusion sets and does not

By admin|2020-09-23T13:13:49+00:00November 8th, 2017|alerts|0 Comments

FDA Recall – Class 2 Device Recall Baxter Amia Automated Peritoneal Dialysis Set with Cassette

Baxter Healthcare Corporation initiated a recall on the Amia Automated Peritoneal Dialysis Set with Cassette. The firm received increased customer complaints for Missing Red Line, Patient Slow Flow, Solution Slow Flow, and Inadequate Drain alerts. The patients and clinics were directed to locate and remove all affected product and to contact Baxter Healthcare Center for

By admin|2020-09-23T13:13:04+00:00November 6th, 2017|alerts|0 Comments