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Pressure Monitoring Device Recall: Medtronic Neurosurgery Issues Correction for Becker and Exacta External Drainage and Monitoring Systems Due to Cracks and/or Leaks in Stopcocks 

Medtronic Neurosurgery is recalling certain Becker and Exacta EDMS due to a risk for cracks and or leaks in device stopcocks.

The FDA has identified this as a Class I recall, the most serious type of recall. This recall involves removing certain devices from where they are used or sold. This device may cause serious injury or death if you continue to use it. 

Questions?

Customers in the U.S. with questions about this recall should contact their Medtronic representative or Medtronic Technical Support at 1-888-826-5603 (reference FA1452).