Urgent Medtronic Neuromodulation INDURA IP Product Recall
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Urgent Medtronic Neuromodulation INDURA IP Product Recall
FDA has issued a Class I Recall on Medtronic Neuromodulation INDURA IP intrathecal catheters, sutureless pump connector revision kits and intrathecal catheter pump segment revision kits.
View full resource at usrecallnews.com
Tags: FDA
Most Recently Shared on October 2, 2008 at 4:16 pm By:
New blog post: Urgent Medtronic Neuromodulation INDURA IP Product Recall http://tinyurl.com/4s3j5u
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