Medical Device Recall: A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.
Medtronic Neuromodulation · January 9, 2025
Reason for Recall
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.
Distribution
Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Canary Islands, Czech Republic, France, Germany, Greece, Ireland, Italy, Netherlands, Norway, Portugal, Puerto Rico, Spain, Sweden, Switzerland, United Kingdom.
States Affected
NATIONWIDE
Quantity Affected
4365 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1506-2025
Status: ongoing
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