| Subject: | Class I Recall of Several Medtronic Intrathecal Catheters and Intrathecal Catheter Revision Kits |
| Category: | Food and Drug Administration (FDA)
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| Published: | Thu, 2 Oct 2008 - 11:00 am |
| Audience: Physical medicine and rehabilitation specialists, anesthesia healthcare professionals, hospital surgical service managersMedtronic and the FDA have notified healthcare professionals of the Class I Recall of several Medtronic intrathecal catheters and intrathecal catheter revision kits used with the implantedMedtronic SyncroMed II, SynchroMed EL, and IsoMed infusion pumps that store and deliver parenteral drugs to the intrathecal space. The specific recalled models... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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