Recall Z-0137-2025— Medtronic Neuromodulation
Class II · Ongoing
Class II FDA medical device recall by Medtronic Neuromodulation, initiated 2024-09-11. FDA's recall record names no specific 510(k) clearance for this event. Product: SynchroMed II Infusion Pump. Product Number: 8637-20. Reason: Potential for error and inability to interrogate pump due to data corruption in the pump memory..
- Recalling firm
- Medtronic Neuromodulation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-09-11
- Firm location
- Minneapolis, MN, United States
Product description
SynchroMed II Infusion Pump. Product Number: 8637-20
Reason for recall
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
Data sourced from openFDA. This site is unofficial and independent of the FDA.