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Medtronic Neuromodulation recalls Clinician Programmer Application (CPA) model A610 Clinician Software Application
Recalled November 10, 2021 · FDA recall Z-0201-2022 · Medtronic Neuromodulation
Hazard
A software anomaly may occur with the clinician programmer application. · FDA Class II
Units
3302
Sold at
Worldwide distribution - US Nationwide distribution and the countries of Australia, New Zealand, Canada, Europe, India, Japan, Korea, Middle East, Latin America, Africa, SE Asia and China.
Description
A software anomaly may occur with the clinician programmer application.
Product
Clinician Programmer Application (CPA) model A610 Clinician Software Application
Manufacturer(s)
Medtronic Neuromodulation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →