cobas e 601 module (cobas 6000 Modular Series system) Part Number: 04745922001
FDA Recall Z-2476-2019 · Posted None
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Recalling FirmRoche Diagnostics Operations, Inc.
Recall StatusTerminated
Product CodeJJE
Date Initiated2019-07-18
Date Terminated2020-06-15
Product Quantity1 unit
Reason for Recall
Quality issue with high pressure solenoid valves may cause inaccurate results.
Firm Action
1. For the cobas 8000 ISE, cobas c 701, and cobas c 702 modules and the cobas c 513 analyzer, stop using these units immediately. Your FES will be in contact with you to replace these affected high pressure solenoid valves immediately.
2. In the event that the high pressure solenoid valves cannot be replaced immediately, for the cobas e 601 module, follow the wash station checks outlined in this Urgent Medical Device Correction (UMDC). Perform these checks once per shift. If these checks show favorable outcomes and quality control results are within range, patient results may be reported. If these checks produce unfavorable outcomes, stop using your cobas e 601 module and call the Roche Support Network Customer Support Center at 1-800-428-2336.
3. Complete the attached fax form and fax or email it according to the instructions on the form.
4. File this Urgent Medical Device Correction (UMDC) for future reference
Please contact the Roche Support Network Customer Support Center, 24 hours a day, seven days a week at 1-800-428-2336 if you have questions about the information contained in this UMDC.
Root Cause
Device Design
Distribution Pattern
State NY MT HI IN MD TX OH KS KY CA FL OR LA MO AK
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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