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Medtronic Neuromodulation recalls A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..
Recalled August 2, 2023 · FDA recall Z-2226-2023 · Medtronic Neuromodulation
Hazard
When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download. · FDA Class II
Units
2 clinician tablets
Sold at
International distribution to the countries of Israel and Serbia.
Description
When an update to the A710 Clinician Programmer software application for the Intellis Neurostimulation System was released, the corresponding version of the A901 Communication Manager software application was not available for download.
Product
A901 Communication Manager Application, used in conjunction with the A710 Clinician Programmer application..
Manufacturer(s)
Medtronic Neuromodulation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →