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Merge Healthcare, Inc. recalls Merge LIS software.
Recalled November 23, 2016 · FDA recall Z-0399-2017 · Merge Healthcare
Hazard
There is a potential for duplicate container numbers to be created for patients. · FDA Class II
Units
413 sites potentially have the affected software
Sold at
Distribution was made nationwide and to the Virgin Islands. Foreign distribution was made to the Bahamas.
Description
There is a potential for duplicate container numbers to be created for patients.
Product
Merge LIS software.
Manufacturer(s)
Merge Healthcare, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →