| Subject: | FDA Class I Classification Given to Baxter's September 2005 Urgent Product Recall for Meridian Hemodialysis Instrument |
| Category: | Food and Drug Administration (FDA)
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| Published: | Fri, 16 Dec 2005 - 10:00 am |
| On December 13, 2005 Baxter Healthcare Corporation announced that the U.S. Food and Drug Administration has classified a September 28, 2005 Urgent Product Recall letter from Baxter to customers regarding the company's Meridian Hemodialysis Instrument, Product Codes 5M5576 and 5M5576R as a Class I recall.
This classification does not require the return of Meridian instruments currently in the market. In the September letter, Baxter directed customers to route arterial blood tubing through only... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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