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The United States Food and Drug Administration Announces Recall of Baxter Healthcare's Colleague Volumetric Infusion Pumps
The US Food and Drug Administration (FDA) issued a class I medical device recall for all models of Baxter Healthcare's Colleague Volumetric Infusion Pumps on 21 July 2005. The affected devices are:
Models 2M8151, 2M8151R, 2M8161, 2M8161R, 2M8153, 2M8153R, 2M8163, and 2M8163R.
Details of the recall can be found on the US FDA website.
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Last Revision Date : 15 December 2012