Medtronic Neuromodulation recalls A820 myPTM Software Application associated with Medtronic Sy
Recalled Product
A820 myPTM Software Application associated with Medtronic SynchroMed Pump and Infusion System.
Hazard / Issue
Product complaints were received describing the A820 myPTM app taking longer than expected for patients to interact with their implantable pump.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: version v.2x, UDI/DI 00763000632793
View official government recall
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