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Siemens Healthcare Diagnostics Inc recalls RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional use in a point-of-care or laboratory environment.
Recalled May 17, 2017 · FDA recall Z-2040-2017 · Siemens Healthcare Diagnostics
Hazard
Potential Patient Demographic Error with Blank Patient ID Field · FDA Class II
Units
159 units
Sold at
Nationwide Foreign: Australia Bangladesh Chile Colombia France Germany Hong Kong India Ireland Japan Latvia Mexico Spain Switzerland Thailand Uruguay
Description
Potential Patient Demographic Error with Blank Patient ID Field
Product
RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional use in a point-of-care or laboratory environment. This system tests blood gases, electrolytes, metabolites, total hemoglobin, and hemoglobin derivatives in arterial, venous, and capillary whole blood samples. Siemens SMN numbers: 10492730, 10696857, 10697306
Manufacturer(s)
Siemens Healthcare Diagnostics Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →