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Siemens Healthcare Diagnostics, Inc. recalls FlexLab Automation Modules
Recalled November 23, 2016 · FDA recall Z-0591-2017 · Siemens Healthcare Diagnostics
Hazard
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
Product
FlexLab Automation Modules
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →