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Medtronic Neuromodulation recalls SynchroMed II Infusion Pump. Product Number: 8637-20
Recalled October 30, 2024 · FDA recall Z-0137-2025 · Medtronic Neuromodulation
Hazard
Potential for error and inability to interrogate pump due to data corruption in the pump memory. · FDA Class II
Units
1 unit
Sold at
US Nationwide distribution in the state of Mississippi.
Description
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
Product
SynchroMed II Infusion Pump. Product Number: 8637-20
Manufacturer(s)
Medtronic Neuromodulation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →