SynchroMed II Infusion Pump. Product Number: 8637-20
Reported: October 30, 2024 Initiated: September 11, 2024 #Z-0137-2025
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.
Details
- Recalling Firm
- Medtronic Neuromodulation
- Units Affected
- 1 unit
- Distribution
- US Nationwide distribution in the state of Mississippi.
- Location
- Minneapolis, MN
Frequently Asked Questions
What product was recalled? ▼
SynchroMed II Infusion Pump. Product Number: 8637-20. Recalled by Medtronic Neuromodulation. Units affected: 1 unit.
Why was this product recalled? ▼
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 30, 2024. Severity: Moderate. Recall number: Z-0137-2025.
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