Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
RAPIDPoint¿ 500 Blood Gas Analyzer with v2.4 software for professional Recalled by Siemens Healthcare Diagnostics Inc Due to Potential Patient Demographic Error with Blank Patient ID...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Siemens Healthcare Diagnostics Inc directly.
Affected Products
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
Quantity: 159 units
Why Was This Recalled?
Potential Patient Demographic Error with Blank Patient ID Field
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Siemens Healthcare Diagnostics Inc
Siemens Healthcare Diagnostics Inc has 75 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report