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Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF) recalls LINQ II Insertable Cardiac Monitor
Recalled March 23, 2022 · FDA recall Z-0782-2022 · Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Hazard
Devices may lose functionality due to susceptibility to moisture ingress. · FDA Class II
Units
8 devices
Sold at
Worldwide distribution - US Nationwide distribution in the states of NJ, NY, PA, and VA. The country of Italy.
Description
Devices may lose functionality due to susceptibility to moisture ingress.
Product
LINQ II Insertable Cardiac Monitor
Manufacturer(s)
Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →