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Medtronic Neuromodulation recalls SynchroMed II implantable drug infusion pump, Model 8637-40,
Recalled April 5, 2017 · FDA recall Z-1694-2017 · Medtronic Neuromodulation
Hazard
Medtronic received a complaint that there was an error code displayed on the programmer when the physician attempted to interrogate an implanted SynchroMed II pump. The error code prevented the physician from updating the pump; however the pump was providing therapy. · FDA Class II
Units
1
Sold at
IL
Description
Medtronic received a complaint that there was an error code displayed on the programmer when the physician attempted to interrogate an implanted SynchroMed II pump. The error code prevented the physician from updating the pump; however the pump was providing therapy.
Product
SynchroMed II implantable drug infusion pump, Model 8637-40,
Manufacturer(s)
Medtronic Neuromodulation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →