| Subject: | Class I Recall of GE Healthcare Aisys and Avance Anesthesia Systems |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 13 May 2010 - 01:00 pm |
| Audience: Anesthesiology healthcare professionals The Food and Drug Administration (FDA) and GE Healthcare are advising healthcare professionals of a Class I Recall of specific lots of the Aisys and Avance Anesthesia Systems. The recalled products are intended to provide general inhalation anesthesia and ventilation support to a wide range of patients. These devices are intended for volume or pressure control ventilation. The product is being recalled because the control board wiring... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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