Medtronic Inc.: Medical Device Recalls in 2016

According to to data from the FDA, there were 2 medical device recalls made by Medtronic Inc. in 2016. See the details of the recalls below.

You can see similar recalls for other firms.

• Reveal LINQ insertable Cardiac Monitor, Model LNQ11. Monitors subcutaneous ECG continuously.
• 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.