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Medtronic Neuromodulation recalls A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.
Recalled April 9, 2025 · FDA recall Z-1506-2025 · Medtronic Neuromodulation
Hazard
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump. · FDA Class II
Units
4365 units
Sold at
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.
Description
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.
Product
A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.
Manufacturer(s)
Medtronic Neuromodulation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →