In case you missed it…

here are a few FDA recalls you might want to know…. 1. Class 1 Recall for Carefusion Alaris Infusion Pump Model 8015  – read notice here  The issue: FDA notified healthcare professionals of a Class I Recall of the Alaris PC unit, model 8015. A component on the PC unit power supply board is causing…

In case you missed it….

…some latest news and initiatives on infection prevention and safety….. “Preventing Infections in Cancer Patients” – CDC is launching a new program called Preventing Infections in Cancer Patients, featuring tools to help both clinicians and patients prevent infections. CDC worked with partners to develop a Basic Infection Control and Prevention Plan for Outpatient Oncology Settings, which…

Class I Recall: Synchromed Implantable Infusion Pumps

A Class I recall has been issued for the SynchroMed II Implantable Infusion Pump, models 8637-20 and 8637-40, distributed between May 2004 and July 8, 2011 manufactured by Medtronics Inc.  The SynchroMed II Pump is indicated when patient therapy requires the chronic infusion of the drugs or fluids. This infusion pump is indicated to deliver…

B. Cereus…. contaminated alcohol swabs, pads & swabsticks?

The FDA released this alert a few days ago: Triad Group Issues a Voluntary Nationwide Recall of All Lots of Alcohol Prep Pads, Alcohol Swabs, and Alcohol Swabsticks Due to Potential Microbial Contamination What??? Are you serious? We use these products to disinfect areas such as skin, injection ports, connectors, etc… prior to injection or…

FDA Alerts/Recall: Several infusion related products

In the past weeks, there have several FDA alerts and recall notices related to products used in infusion therapy. Here are some of the products. Class I Recall: CareFusion Corporation, Alaris PC Units (Model 8015) Reason for Recall: Under certain wireless network conditions, a communication error can occur, which freezes the PC Unit screen. This…

The Good, The Bad and Drug Shortages.

It doesn’t take a rocket scientist to know that when you don’t have enough of a good thing, bad things can happen. This is the case with the on-going drug shortages and the resulting potential issues that affect the care we provide and patient safety concerns. The ISMP (Institute for Safe Medication Practices) recently released…

FDA Class I Recall: Symbiq Infusion Pumps

There is an FDA Class I recall of Symbig Infusion Pumps One channel, model 16026 and Dual channels, model 16027 made by Hospira due to the potential for unrestricted flow of fluid or medication if the administration set (cassette) is removed before the cassette carriage fully opens and the slide/roller clamp is not closed. Additionally,…

FDA Safety Alert on Nimodipine: Not for IV use

Nimodipine is a medication intended to be given in a critical care setting to treat neurologic complications from subarachnoid hemorrhage and is only available as a capsule. The U.S. Food and Drug Administration (FDA) is alerting healthcare professionals that nimodipine capsules should be given ONLY by mouth or through a feeding tube (nasogastric tube). This…

FDA Infusion Pump Improvement Initiative

External infusion pumps, commonly called “infusion pumps”, including large volume, patient-controlled analgesia (PCA) , elastomeric , syringe , enteral, and insulin pumps, are used worldwide in healthcare facilities such as hospitals, and in the home.  Infusion pumps have contributed to improvements in patient care, allowing for a greater level of control, accuracy, and precision in…