The Recall Desk

FDA (Devices) recall action 71073

Siemens Healthcare Diagnostics, Inc recalled 2 products on 2015-07-08

The FDA (Devices) publishes a recall like this one as 2 separate product records. They share a firm, a date and a cause; this page is all of them in one place, so the scale of the action is visible rather than spread across 2 pages.

Products
2
Announced
2015-07-08
Critical
0
Units
2,835

Why these products were recalled

D50 and D51 Diagnostic error codes are not functional.

D50 and D51 diagnostic error codes are not functional.

The agency’s own wording, quoted from the enforcement report.

The unit total adds up the quantities the agency stated for each product. Where a product record gave no figure, or gave a weight rather than a count, it contributes nothing — so the real total is at least this, never less.

States named across these recalls

1–2 of 2

  • HighFDA (Devices)··2015-07-08

    Siemens Rapidlab 1260 Blood Gas Analyzer Recalled for Diagnostic Error Codes

    Siemens Healthcare Diagnostics is recalling 122 Rapidlab 1260 blood gas analyzers because specific diagnostic error codes are not functional.

    Product
    The Rapidlab 1260 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples.
    Category
    Distribution
    1 state
  • HighFDA (Devices)··2015-07-08

    Siemens Rapidlab 1265 Blood Gas Analyzer Recalled for Diagnostic Error Code Failure

    Siemens Healthcare Diagnostics is recalling 2,713 Rapidlab 1265 blood gas analyzers because specific diagnostic error codes are not functional.

    Product
    The Rapidlab 1265 system is a blood gas analyzer used for laboratory testing of blood gases, electrolytes, metabolites and CO-oximetry in arterial, venous and capillary whole blood samples.
    Category
    Distribution
    1 state