cobas p 612 pre-analytical system; Pre-analytical sample handling that includes de-capping, Aliquotting and sorting of samples for analysis.
FDA Recall Z-1090-2017 · Posted 2017-01-24
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Recalling FirmRoche Diagnostics Corporation
Recall StatusTerminated
Product CodeJQP
Date Initiated2016-12-27
Date Terminated2017-08-04
Product Quantity5
Firm Action
On 12/27/2016, URGENT MEDICAL DEVICE CORRECTION notifications were sent to the affected Consignees via courier fax or email. The recall notifications included a description of the reason for the recall, affected product, consignee responsibilities, and instructions for responding to the formal recall notification.
The cobas p 612 pre-analytical system (63x) software is being revised to correct the aspiration process. We anticipate this new version (2.0.4) to be available during Quarter 1 2017.
For now, discontinue using disposable non-filter tips for Aliquotting on your cobas p 612 pre-analytical system (63x). You will be contacted by a Roche Field Engineering Specialist (FES) about modifying your system to allow for the use of disposable filter tips. Filter tips will be provided at the time of service.
Actions Required
" Immediately discontinue using disposable non-filter tips for Aliquotting on your cobas p 612 pre-analytical system (63x).
" Complete the enclosed faxback form and fax it to number 1-877-906-8982 or email it to [email protected].
" Provide copies of this UMDC to other clinicians who may need to be aware of this software issue.
" If your facility has distributed the affected product to another site, please ensure this UMDC is provided to that site.
" File this UMDC for future reference.
Please contact the Roche Support Network Customer Support Center at 1-800-428-2336, 24 hours a day/7 days a week, if you have questions about the information contained in this UMDC.
Root Cause
Software design
Distribution Pattern
TX and WA
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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