| Subject: | FDA Updates Information on Baxter Healthcare Colleague Volumetric Infusion Pump and Baxter Healthcare Syndeo Patient Controlled Analgesic Syringe Pump |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 13 Jul 2006 - 12:00 am |
| Audience: Hospital nursing supervisory personnel and risk managers
The FDA has notified healthcare professionals that Baxter Healthcare will stop manufacturing and distributing all models of Colleague Volumetric Infusion Pump and Syndeo Patient Controlled Analgesic Syringe Pump until the company corrects manufacturing deficiencies and is in compliance with FDA's current good manufacturing practice requirements and the Quality System regulation for devices.
The FDA will allow the firm to... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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