FDA-Device2024-10-30Class II
SynchroMed II Infusion Pump. Product Number: 8637-20
Medtronic Neuromodulation
Hazard
Potential for error and inability to interrogate pump due to data corruption in the pump memory.
Sold states
US Nationwide distribution in the state of Mississippi.
Affected count
1 unit
Manufactured in
7000 Central Ave Ne, N/A, Minneapolis, MN, United States
Products
SynchroMed II Infusion Pump. Product Number: 8637-20
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0137-2025Don't want to check this manually?
We email you a Sunday digest of new federal recalls relevant to parents — free, no credit card. Or upgrade to as-it-happens alerts for the brands you actually own.
Get the Sunday Brief