FDA Device recall Z-0378-2018
Brand Name: ¿ cobas c 6000 MODULAR Series System e 601 ¿ cobas c 8000 MODULAR Series System - e 602 ¿ Roche / Hitachi MODULAR Analytics Com…
- FDA Device
- Class II
- terminated
- Published 2018-01-24
On 2018-01-24 the FDA classified a Class II recall of Brand Name: ¿ cobas c 6000 MODULAR Series System e 601 ¿ cobas c 8000 MODULAR Series System - e 602 ¿ Roche / Hitachi MODULAR Analytics Com… by Roche Diagnostics, citing 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 limitati….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0378-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-06-29 |
| Published | 2018-01-24 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Roche Diagnostics |
| Distribution | US |
Product
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.
Identifiers
| code_info | Serial Number 2072-26 27P6-20 15S2-20 2717-18 2719-02 1544-11 1686-03 1534-12 1698-04 1549-04 2275-12 2263-…Serial Number 2072-26 27P6-20 15S2-20 2717-18 2719-02 1544-11 1686-03 1534-12 1698-04 1549-04 2275-12 2263-16 2263-17 2497-16 1849-01 1570-15 26F0-17 2256-18 2564-30 2850-05 2384-12 2384-18 2399-08 2230-19 2230-20 2379-14 2381-02 27Z8-01 2058-22 1909-13 1909-01 27V5-20 15U5-18 2308-01 2087-07 1984-05 1985-07 26D3-30 2497-01 1861-18 1861-19 26D0-27 26D1-21 1480-14 1480-15 1488-01 1488-02 26C3-12 26F0-19 26F0-27 26D9-24 2107-35 2348-12 2348-13 1423-16 2237-18 2240-09 2240-10 16J8-05 16J8-06 16L7-20 16K2-17 16K2-18 16K2-19 16K2-20 16K3-01 16K3-06 16K3-07 16K3-08 16K3-09 16L4-03 16L4-04 26D1-25 26D1-26 26D1-28 26D1-29 2328-03 2437-13 2072-29 2072-30 2064-12 1931-11 2080-35 1936-08 2049-15 27Z0-09 27Z0-10 1911-11 2581-18 2062-14 2074-05 1430-16 1430-17 1691-17 1691-18 1985-13 1989-19 1739-19 2578-25 13B8-12 1169-06 1169-08 1169-09 1211-16 1211-17 1211-18 1224-10 1458-04 2543-10 27J6 |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0378-2018%22
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