Medtronic medication pumps are widely used to deliver pain medication, anti-spasm medication and other prescriptions directly into the spinal cord. And the FDA has determined that these pumps can cause serious harm. The FDA has issued a Class 1 recall.
The SynchroMed II implantable pumps, models 8637-20 and 8637-40 are the subject of the recall which has been reported here. A Class 1 recall means that these pumps have a reasonable probability of causing serious adverse health consequences or death. The pumps are failing, apparently due to a defective design relating to the battery.
These pumps are surgically implanted under the skin with delivery tubes placed to the point of delivery. Medtronic is not recommending that the pumps be removed and replaced at this point, says MedPage Today.
If you or a loved one has experienced a failure related to one of these pain pumps, or if you have one of these pumps implanted, you should contact our office to discuss your legal rights. Contact us at 314-721-8833 or at www.stlmedicalmalpractice.com.
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