| Subject: | CareFusion Issues Update Regarding Previously Disclosed Recall of the Alaris System |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 31 Jul 2009 - 11:00 am |
| CareFusion Corporation has issued an update regarding its previous recall of the Alaris System.According to the company, the affected devices have one or more failures associated with the Occlusion Warning Message, Syringe Volume Warning Message, Electrostatic Discharge protection circuitry, and Fluid Ingress into the device's pumping mechanism. This recall also updates the labeling for the Inter Unit Interface (IUI) connectors on the Alaris System. The potential risks may lead... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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