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Medtronic Inc. recalls CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, th
Recalled October 5, 2016 · FDA recall Z-2898-2016 · Medtronic
Hazard
Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error. · FDA Class II
Units
33 units
Sold at
Nationwide Distribution to TN, MN, and WA
Description
Medtronic MiniMed is recalling the CareLink iPro Therapy Management Software due to a time stamp error.
Product
CareLink iPro Version 1.10, Catalog No. MMT-7340 With data obtained from the iPro2 recorder and blood glucose meter, the CareLink iPro software retrospectively calibrates sensor data and provides reports of continuous glucose information. CareLink iPro reports show up to seven calendar days of study data. The reports are created in PDF format, so they can easily be printed or stored electronically.
Manufacturer(s)
Medtronic Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →