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Siemens Healthcare Diagnostics Recalls

692 recalls on record · July 4, 2012 to August 12, 2026 · Medical Devices

Recalls by year

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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.

May 8, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc recalls Atellica IM aTG (500 test kit) Siemens Material Number (SMN): 10995462
Hazard: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in 316 and lower and Atellica IM aTG kit lots ending in 317 and lower when compared to the standardization to World Health Organization (WHO) Reference Preparation MRC 65/93 stated in the Instructions for Use (IFU).
May 8, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc recalls Siemens Atellica IM aTG (100 test kit) Siemens Material Number (SMN): 10995461
Hazard: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in 316 and lower and Atellica IM aTG kit lots ending in 317 and lower when compared to the standardization to World Health Organization (WHO) Reference Preparation MRC 65/93 stated in the Instructions for Use (IFU).
May 8, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc recalls SiemensADVIA Centaur aTG (500 test kit) Siemens Material Number (SMN): 10492399
Hazard: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in 316 and lower and Atellica IM aTG kit lots ending in 317 and lower when compared to the standardization to World Health Organization (WHO) Reference Preparation MRC 65/93 stated in the Instructions for Use (IFU).
May 8, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc recalls Siemens ADVIA Centaur aTG (100 test kit) Siemens Material Number (SMN): 10492398
Hazard: Positive bias anti-thyroglobulin with ADVIA Centaur aTG kit lots ending in 316 and lower and Atellica IM aTG kit lots ending in 317 and lower when compared to the standardization to World Health Organization (WHO) Reference Preparation MRC 65/93 stated in the Instructions for Use (IFU).
April 24, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls syngo Lab Data Manager System - Product Usage: syngo Lab Data Manager is a clinical system that assists medical laborato
Hazard: Software Issues.
March 27, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista 1500, Analyzer, chemistry Model no. 10444801
Hazard: When the Millipore Water Purification Module Progard Pretreatment Packs are used with Dimension Vista Triglyceride assay, patient and QC triglyceride results may be erroneously elevated as a result of contamination.
March 27, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista 500, Analyzer, chemistry Model no. 10284473
Hazard: When the Millipore Water Purification Module Progard Pretreatment Packs are used with Dimension Vista Triglyceride assay, patient and QC triglyceride results may be erroneously elevated as a result of contamination.
February 6, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica Sample Handler Prime. In vitro diagnostic testing of clinical specimens - Siemens Material Number (SMN): 110690
Hazard: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2 and lower in: Atellica¿ IM 1300 Analyzer Atellica¿ IM 1600 Analyzer;Atellica¿ CH 930 Analyzer; Atellica¿ Sample Handler Prime
February 6, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH 930 Analyzer. In vitro diagnostic testing of clinical specimens Siemens Material Number (SMN): 1 067000 - P
Hazard: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2 and lower in: Atellica¿ IM 1300 Analyzer Atellica¿ IM 1600 Analyzer;Atellica¿ CH 930 Analyzer; Atellica¿ Sample Handler Prime
February 6, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1600 Analyzer: In vitro diagnostic testing of clinical specimens - Product Usage: The Atellica Solution is
Hazard: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2 and lower in: Atellica¿ IM 1300 Analyzer Atellica¿ IM 1600 Analyzer;Atellica¿ CH 930 Analyzer; Atellica¿ Sample Handler Prime
February 6, 2019Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1300 Analyzer. In vitro diagnostic testing of clinical specimens. Siemens Material Number (SMN): 1066001 - P
Hazard: Multiple Issues Identified in Atellica Solution System Software in V 1.14.2 and lower in: Atellica¿ IM 1300 Analyzer Atellica¿ IM 1600 Analyzer;Atellica¿ CH 930 Analyzer; Atellica¿ Sample Handler Prime
December 26, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista 1500, Model No. 10444801 an in vitro diagnostic device intended to duplicate manual analytical procedure
Hazard: 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 while the instrument is aliquotting the sample, the Dimension Vista instrument may continue to deliver the cancelled sample or vial contents to the aliquot well(s). Future samples may be assigned to the same aliquot well(s) and become contaminated with the existing contents or overflow of the aliquot well may occur potentially contaminating a surrounding well(s). This issue only occurs when an operator manually cancels a test(s) for calibration, quality control (QC) or patient sample while the instrument is in the process of aliquotting the sample.
December 26, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista 500, model no. 10284473 an in vitro diagnostic device intended to duplicate manual analytical procedures
Hazard: 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 while the instrument is aliquotting the sample, the Dimension Vista instrument may continue to deliver the cancelled sample or vial contents to the aliquot well(s). Future samples may be assigned to the same aliquot well(s) and become contaminated with the existing contents or overflow of the aliquot well may occur potentially contaminating a surrounding well(s). This issue only occurs when an operator manually cancels a test(s) for calibration, quality control (QC) or patient sample while the instrument is in the process of aliquotting the sample.
December 5, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge, an in vitro diagnostic test for the quantitative mea
Hazard: 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 Lactic Acid (LA). The magnitude of the elevation may be variable. Both quality control and patient samples may be impacted. Incomplete removal of residual lactate dehydrogenase, a component of the LA reagent, has been identified as the cause of the potentially elevated result. A falsely elevated result for lactate dehydrogenase may lead to additional investigations to determine the etiology of tissue damage. Results would be correlated with clinical history and presentation in addition to other diagnostic laboratory testing.
November 21, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Vista Lipase Flex Reagent Cartridge, Model Number 10461745 Product Usage: Dimension Vista - The LIPL metho
Hazard: There is lot to lot variability for QC and patient results when using the identified reagent cartridge lots.
November 21, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Lipase Flex Reagent Cartridge, Model Number 10460277 Product Usage: Dimension - The LIPL method is an in v
Hazard: There is lot to lot variability for QC and patient results when using the identified reagent cartridge lots.
November 14, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Dimension Thermal Chamber Motor Cable located in the following models: Model/UDI Number: Dimension¿ EXL 200 0063041459
Hazard: 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 in a potential electrical shock
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls STREAMLAB - REFRIGERATED STORAGE MODULE 15000
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls STREAMLAB - REFRIGERATED STORAGE MODULE 9000
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls STREAMLAB CORE UNIT / LYNX WITH IOM
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls APTIO RACK OUTPUT MODULE
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls APTIO 9000 REFRIGERATED STORAGE MODULE
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls APTIO 15000 REFRIGERATED STORAGE MODULE
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls APTIO CENTRIFUGE MODULE
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls APTIO RACK INPUT MODULE
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 31, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls APTIO INPUT/OUTPUT MODULE
Hazard: The modules may have been shipped without a warning label for potential risk of interference to pacemaker functionality.
October 24, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica CH 930 Analyzer (SMN 11067000) . The Atellica" Solution is a multi-component system for in vitro diagnostic te
Hazard: 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 Ancillary Packs when more than one (1) lot of specific Reagent kits are loaded on the analyzer at the same time. 2. Sample barcodes may be incorrectly read 3. The Atellica IM 1300 Analyzer and Atellica IM 1600 Analyzer may not run CEA dilutions at 50x and 100x. The Analyzer may post a Sample Integrity Error when 50x or 100x dilutions are ordered for Carcinoembryonic Antigen (CEA). Dilution factors lower than 50x and neat samples are not affected by this behavior. 4. The Atellica CH 930 Analyzer may continue to display the default reporting units after the reporting units have been changed. 5. The Atellica CH 930 Analyzer may not display results for sample if certain assays are configured to auto-dilute results above or below the assay measuring interval.
October 24, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1600 Analyzer (SMN 11066000). The Atellica" Solution is a multi-component system for in vitro diagnostic te
Hazard: 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 Ancillary Packs when more than one (1) lot of specific Reagent kits are loaded on the analyzer at the same time. 2. Sample barcodes may be incorrectly read 3. The Atellica IM 1300 Analyzer and Atellica IM 1600 Analyzer may not run CEA dilutions at 50x and 100x. The Analyzer may post a Sample Integrity Error when 50x or 100x dilutions are ordered for Carcinoembryonic Antigen (CEA). Dilution factors lower than 50x and neat samples are not affected by this behavior. 4. The Atellica CH 930 Analyzer may continue to display the default reporting units after the reporting units have been changed. 5. The Atellica CH 930 Analyzer may not display results for sample if certain assays are configured to auto-dilute results above or below the assay measuring interval.
October 24, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM 1300 Analyzer (SMN 11066001). The Atellica" Solution is a multi-component system for in vitro diagnostic
Hazard: 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 Ancillary Packs when more than one (1) lot of specific Reagent kits are loaded on the analyzer at the same time. 2. Sample barcodes may be incorrectly read 3. The Atellica IM 1300 Analyzer and Atellica IM 1600 Analyzer may not run CEA dilutions at 50x and 100x. The Analyzer may post a Sample Integrity Error when 50x or 100x dilutions are ordered for Carcinoembryonic Antigen (CEA). Dilution factors lower than 50x and neat samples are not affected by this behavior. 4. The Atellica CH 930 Analyzer may continue to display the default reporting units after the reporting units have been changed. 5. The Atellica CH 930 Analyzer may not display results for sample if certain assays are configured to auto-dilute results above or below the assay measuring interval.
October 24, 2018Medical DevicesFDA
Siemens Healthcare Diagnostics, Inc. recalls Atellica Sample Handler Additional (SMN 11069004). The Atellica" Solution is a multi-component system for in vitro di
Hazard: 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 Ancillary Packs when more than one (1) lot of specific Reagent kits are loaded on the analyzer at the same time. 2. Sample barcodes may be incorrectly read 3. The Atellica IM 1300 Analyzer and Atellica IM 1600 Analyzer may not run CEA dilutions at 50x and 100x. The Analyzer may post a Sample Integrity Error when 50x or 100x dilutions are ordered for Carcinoembryonic Antigen (CEA). Dilution factors lower than 50x and neat samples are not affected by this behavior. 4. The Atellica CH 930 Analyzer may continue to display the default reporting units after the reporting units have been changed. 5. The Atellica CH 930 Analyzer may not display results for sample if certain assays are configured to auto-dilute results above or below the assay measuring interval.