The U.S. Food and Drug Administration has issued a Class I recall, the agency’s most serious, for a Medtronic device used to temporarily drain spinal fluid from patients after surgery for a thoracic ...
Medtronic is recalling more than 45,000 cerebrospinal fluid (CSF) drainage and sampling tubes from the U.S. over an issue linked to 26 injuries. The Food and Drug Administration, which published ...
Medtronic Neurosurgery is recalling 45,176 drainage systems because catheters might disconnect from patient line stopcock connectors. There have been 26 reported injuries, the FDA said March 7. Six ...
Please provide your email address to receive an email when new articles are posted on . The FDA announced the Class I recall of the Medtronic Neurosurgery, Medtronic Duet External Drainage and ...
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