Medtronic baclofen pump recall

medtronic baclofen pump recall

Part of the SynchroMed II system, SynchroMed EL and SynchroMed II pumps store and deliver pain medication via a catheter implanted under the skin. Medtronic is updating the software for its SynchroMed implantable infusion pumps due to a software issue that could cause the devices. Class I Recall of Certain Medtronic Infusion Pumps and ziconotide for the treatment of chronic pain, intrathecal baclofen for severe spasticity. Results 1 - 10 of 71 Medtronic SynchroMed® II Implantable Drug Infusion Pump, Model , The implantable 23, 2, 05/08/, Medtronic. medtronic baclofen pump recall

Medtronic baclofen pump recall - mistaken

Medtronic made a software change to the Synchromed II application contained on the Model software application card. Medtronic is updating the Model software application card as well as the SynchroMed Infusion System labeling to mitigate the risk of the potential for clinically relevant effects of over-delivery of unintended drug during the full system priming bolus procedure. Or the catheters become clogged. It is commonly used when a patient does not respond to oral pain medications or suffers reactions. Medtronic is not recommending prophylactic replacement of pumps due to the low projected rate of occurrence of this issue. The SynchroMed EL pump does not provide an alarm to alert the patient or clinician to a stalled motor condition. Zip Code. This communication provides information and instructions regarding go here recall of specific lots of Medtronic intrathecal catheter kits and revision kits. This document provides a summary of the new information related to potential effects of an MRI scan on the Meftronic pump. With an updated browser, you will have a better Medtronic website experience. Now, patients are fighting back redall lawsuits against Medtronic over claims that the medical device company made a defective device and failed to warn consumers of the risks. Additionally, the catheter can be accessed, also subcutaneously, by injecting dye to aspirate the tube or check for possible occlusions that may reduce the programmed delivery of medication.

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