Devices

Device Recall 8596SC Intrathecal Catheter Pump Segment Revision Kit

Model / Serial
Lot Numbers: N131154001, N131154003, N131154004, N131154008, N131154009, N131154010, N131154013, N131154016, N131154017, N130483001, N130483004, N130483006, N130483011, N130483012, N130483013, N130483014, N130483015 and N130483021.
Product Classification
General Hospital and Personal Use Devices
Device Class
3
Implanted device?
Yes
Distribution
Nationwide Distribution including states of MI, OR, IN, NY, FL, PA, MN, TX, CO and UT.
Product Description
Medtronic Intrathecal Catheter Pump Segment Revision Kit; Programmable implanted infusion pump; Model Number: 8596SC; Packaged with catheter model number 8731 or 8731SC.
Manufacturer
Medtronic Neuromodulation
1 Event
- Recall of Device Recall 8596SC Intrathecal Catheter Pump Segment Revision Kit

Manufacturer

Medtronic Neuromodulation

Manufacturer Address
Medtronic Neuromodulation, 800 53rd Ave NE, PO Box 1250, Minneapolis MN 55440-1250
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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