BEUDAMED
    FDA Recall Terminated

    Brand Name: cobas c 6000 MODULAR Series System e 601 cobas c 8000 MODULAR Series System - e 602 Roche / Hitachi MODULAR Analytics Combination System Model/Catalog/Part Number: MODULAR Analytics E 170 03022109001 03023109973 03739040001 03739040692 05023572001 05023599001 cobas e 601 module 04745922001 04745922692 05036348001 05036348692 05860652001 cobas e 602 module 05990378001 The Roche/Hitachi MODULAR Analytics System (E170) is a fully automated, random-access, software- controlled system for immunoassay and photometric analysis intended for qualitative and quantitative in vitro determinations using a wide variety of tests. The cobas 6000 series (e 601) is a fully automated, random-access, software-controlled system for immunoassay and photometric analysis intended for qualitative and quantitative in vitro determinations using a wide variety of tests. It is optimized for high throughput workloads in the professional environment using a combination of Ion selective electrodes (ISE), a photometric analysis unit an immunoassay analysis module. The cobas 8000 Modular Analyze Series (e602) is a fully automated system for Clinical chemistry analysis, intended for the in vitro qualitative and quantitative determination of analytes in body fluids. It is optimized for high throughput workloads in the professional environment using a combination of ion selective electrodes (ISE) and a photometric analysis unit.

    Recall: Z-0378-2018 · Initiated June 29, 2017

    Recall

    Recall Number
    Z-0378-2018
    Event Number
    78760
    Firm
    Roche Diagnostics Corporation
    FEI Number
    1823260
    Product Code
    JJE
    Status
    Terminated
    Root Cause
    Software design
    Initiated
    June 29, 2017
    Posted
    January 16, 2018
    Terminated
    January 24, 2020
    Address
    9115 Hague Rd, Indianapolis, IN, 46256-1025

    Description

    Brand Name: cobas c 6000 MODULAR Series System e 601 cobas c 8000 MODULAR Series System - e 602 Roche / Hitachi MODULAR Analytics Combination System Model/Catalog/Part Number: MODULAR Analytics E 170 03022109001 03023109973 03739040001 03739040692 05023572001 05023599001 cobas e 601 module 04745922001 04745922692 05036348001 05036348692 05860652001 cobas e 602 module 05990378001 The Roche/Hitachi MODULAR Analytics System (E170) is a fully automated, random-access, software- controlled system for immunoassay and photometric analysis intended for qualitative and quantitative in vitro determinations using a wide variety of tests. The cobas 6000 series (e 601) is a fully automated, random-access, software-controlled system for immunoassay and photometric analysis intended for qualitative and quantitative in vitro determinations using a wide variety of tests. It is optimized for high throughput workloads in the professional environment using a combination of Ion selective electrodes (ISE), a photometric analysis unit an immunoassay analysis module. The cobas 8000 Modular Analyze Series (e602) is a fully automated system for Clinical chemistry analysis, intended for the in vitro qualitative and quantitative determination of analytes in body fluids. It is optimized for high throughput workloads in the professional environment using a combination of ion selective electrodes (ISE) and a photometric analysis unit.

    Reason

    Roche has confirmed that a possible sample mismatch issue may occur on the MODULAR ANALYTICS E 170 module, cobas e 601 analyzer, or cobas e 602 analyzer due to a software limitation.

    Action

    Roche sent an Urgent Medical Device Correction (UMDC) sent via UPS Ground (receipt required) dated July 6, 2017, and an amended UMDC on August 31 ,2017. All consignees will be notified by Urgent Medical Device Correction sent via UPS Ground (receipt required). Customers/consignees were instructed the following: If the Tip/Cup pick up error alarm is issued then followed by the Abnormal L2-line Movement alarm on your MODULAR ANALYTICS E 170 module, cobas e 601 analyzer, or cobas e 602 analyzer, after which the system goes into Sampling Stop, follow the steps in this UMDC and the appropriate How to Identify Potentially Mismatched Sample Results within the enclosed document. For further questions, please call (317) 521-4343.

    Distribution

    USA (nationwide) Distribution

    Quantity

    2517