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Siemens Healthcare Diagnostics, Inc. recalls Dimension IRON Flex reagent cartridges
Recalled November 23, 2016 · FDA recall Z-0402-2017 · Siemens Healthcare Diagnostics
Hazard
Siemens Healthcare Diagnostics has become aware of deferoxamine interference with Dimension and Dimension Vista IRON assays at a different concentration than listed in the Instructions for Use (IFU). · FDA Class III
Units
38,230 cartridges
Sold at
Distributed Nationwide
Description
Siemens Healthcare Diagnostics has become aware of deferoxamine interference with Dimension and Dimension Vista IRON assays at a different concentration than listed in the Instructions for Use (IFU).
Product
Dimension IRON Flex reagent cartridges
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →