Overview of recall records associated with Siemens Healthcare Diagnostics, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 324, Class III: 2.
Siemens Healthcare Diagnostics has identified an issue with Dimension Vista software v.3.7 and v.3.8.1 that may result in aliquot well contamination. If a test is cancelled by the operator…
Siemens Healthcare Diagnostics has identified an issue with Dimension Vista software v.3.7 and v.3.8.1 that may result in aliquot well contamination. If a test is cancelled by the operator…
Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate Dehydrogenase (LDI) may exhibit an erroneously elevated result when the preceding assay in the reaction cuvette is…
There is lot to lot variability for QC and patient results when using the identified reagent cartridge lots.
There is lot to lot variability for QC and patient results when using the identified reagent cartridge lots.
Thermal chamber motors have electrical cables with single insulation rather than the required double insulation. There is no exposed current due to the single insulation that could result…
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
Atellica Solution system software (SW) version 1.13 and lower, five (5) behavioral issues were identified: 1. Reagent Lock may not work as intended with Primary Reagent ReadyPacks and…
A potential bias was identified with certain kits compared to the internal standards.
Atellica Solution system software (SW) version 1.13 and lower, five (5) behavioral issues were identified: 1. Reagent Lock may not work as intended with Primary Reagent ReadyPacks and…
Atellica Solution system software (SW) version 1.13 and lower, five (5) behavioral issues were identified: 1. Reagent Lock may not work as intended with Primary Reagent ReadyPacks and…
A potential bias was identified with certain kits compared to the internal standards.
Atellica Solution system software (SW) version 1.13 and lower, five (5) behavioral issues were identified: 1. Reagent Lock may not work as intended with Primary Reagent ReadyPacks and…
Atellica Solution system software (SW) version 1.13 and lower, five (5) behavioral issues were identified: 1. Reagent Lock may not work as intended with Primary Reagent ReadyPacks and…
Atellica Solution system software (SW) version 1.13 and lower, five (5) behavioral issues were identified: 1. Reagent Lock may not work as intended with Primary Reagent ReadyPacks and…
A potential bias was identified with certain kits compared to the internal standards.
This page summarizes recall records in which the official source identifies Siemens Healthcare Diagnostics, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
