| Subject: | Class I Recall of Baxter Colleague Single and Triple Channel Volumetric Infusion Pumps |
| Category: | Food and Drug Administration (FDA)
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| Published: | Wed, 11 Mar 2009 - 06:00 pm |
| The FDA is notifying health care professionals of a Class I Recall of Baxter's Colleague Single and Triple Channel Volumetric Infusion Pumps. According to the FDA, the company identified software and battery usage failures that result in a delay in or interruption of infusion that may cause serious injury and/or death. The model numbers for the recalled pumps are:Mono 2M8151 and 2M8153CX 2M8161 and 2M8163XE 2M9161and 2M9163These products were manufactured and distributed from February... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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