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Medical Information Technology, Inc. recalls MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Informat
Recalled May 29, 2013 · FDA recall Z-1365-2013 · Medical Information Technology
Hazard
Incorrect transmission of laboratory results. · FDA Class II
Units
56 devices
Sold at
Worldwide Distribution - USA, including Puerto Rico and the country of Canada.
Description
Incorrect transmission of laboratory results.
Product
MEDITECH Bi-Directional interactive Communication Analyzer Interface; Integrates with MEDITECH's Laboratory Information System (LIS) with Other Vendor systems to manage the transfer of patient results and demographic information.
Manufacturer(s)
Medical Information Technology, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →