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Fresenius Kabi Recalls Volumat MC Agilia Infusion Pump and Vigilant Agilia Drug Library

The FDA has identified this as a Class I recall, the most serious type of recall.  Use of these devices may cause serious injuries or death. Recalled Product Volumat MC Agilia Infusion System and Vigilant Drug LibraryModelsVolumat MC Agilia Z021135, Software Versions 1.7 and 1.9aVigilant Drug Library Z073476, Software Versions 1.0 and 1.1Lot Numbers: AllManufacturing

By |2020-09-23T13:15:48+00:00August 15th, 2019|alerts|0 Comments

Hospira Issues Voluntary Nationwide Recall

Hospira, Inc., a Pfizer company, is voluntarily recalling 8 lots of Hospira’s Daptomycin for Injection 500 mg, Lyophilized Powder For Solution, Single Dose Vial (NDC 0409-0106-01) to the Hospital/Retail level. The product is being recalled due to adverse event reports indicative of infusion reactions. Daptomycin for Injection has been associated with reports of adverse events indicative of

By |2020-09-23T12:05:24+00:00July 18th, 2018|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 |2020-09-23T13:13:04+00:00November 6th, 2017|alerts|0 Comments