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Siemens Healthcare Diagnostics, Inc. recalls Aptio Automation Modules
Recalled November 23, 2016 · FDA recall Z-0590-2017 · Siemens Healthcare Diagnostics
Hazard
Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems. · FDA Class II
Units
448 units
Sold at
Distributed Nationwide and to the following countries: Australia, Azerbaijan, Bahrain, Bangladesh, Belgium, Brazil, Canada, Czech Republic, Denmark, Egypt, Germany, Greece, Indonesia, Italy, Kingdom Saudi Arabia, Lebanon, Malaysia, P.R. China, Philippines, Portugal, Qatar, Republic Korea, Saudi Arabia, Spain, Sweden, Switzerland, Taiwan, Turkey, U.A.E., United Kingdom, Vietnam
Description
Possible overheating of power cord plugs used to connect to FlexLab and Aptio Automation systems.
Product
Aptio Automation Modules
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →