| Subject: | Class I Recall of HomeChoice and HomeChoice PRO Automated Peritoneal Dialysis Systems |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 4 Mar 2010 - 02:00 pm |
| Audience: Nephrology healthcare professionals, patients The Food and Drug Administration (FDA) and Baxter have notified healthcare professionals of a Class I recall of the HomeChoice and HomeChoice PRO Automated Peritoneal Dialysis Systems, which are prescription medical devices used to treat pediatric and adult patients with kidney failure. Reports of serious injuries and at least one death have been associated with increased Intraperitoneal Volume (IIPV). IIPV may result in serious injury or... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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