Class II
Medical Device Recall: SynchroMed II Infusion Pump. Product Number: 8637-20
Medtronic Neuromodulation · September 11, 2024
Reason for Recall
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
Distribution
US Nationwide distribution in the state of Mississippi.
States Affected
NATIONWIDE
Quantity Affected
1 unit
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0137-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.