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Merge Healthcare, Inc. recalls Merge Hemo, Software packages 10.2, 10.3, and 10.4
Recalled September 8, 2021 · FDA recall Z-2387-2021 · Merge Healthcare
Hazard
The firm identified a safety issue affecting the software associated with Merge Hemo versions 9.x and 10.x, used in combination with an HL7 lab interface. · FDA Class II
Units
326 units
Sold at
US distribution
Description
The firm identified a safety issue affecting the software associated with Merge Hemo versions 9.x and 10.x, used in combination with an HL7 lab interface.
Product
Merge Hemo, Software packages 10.2, 10.3, and 10.4
Manufacturer(s)
Merge Healthcare, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →