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Siemens Healthcare Diagnostics, Inc. recalls Atellica CH Reaction Ring Segment, SMN 11099326, UDI 00630414596143
Recalled March 11, 2020 · FDA recall Z-1421-2020 · Siemens Healthcare Diagnostics
Hazard
Some lots ending in "17", "18", "19", or higher may have cuvette defects allowing water from the water bath to contaminate the interior of the cuvette, which may falsely elevate or depress sample results. · FDA Class II
Units
3559
Sold at
Domestic distribution nationwide. Worldwide foreign distribution.
Description
Some lots ending in "17", "18", "19", or higher may have cuvette defects allowing water from the water bath to contaminate the interior of the cuvette, which may falsely elevate or depress sample results.
Product
Atellica CH Reaction Ring Segment, SMN 11099326, UDI 00630414596143
Manufacturer(s)
Siemens Healthcare Diagnostics, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →