cobas HCYS, Homocysteine Enzymatic Assay, Material Number REF 06542921190, for use on cobas c 701/702, in vitro test for total L-homocysteine
FDA Recall Z-0489-2025 · Posted 2024-11-19
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Recalling FirmRoche Diagnostics Operations, Inc.
Recall StatusOpen, Classified
Product CodeLPS
Date Initiated2024-10-17
Product Quantity458 units
Reason for Recall
Abnormal calibration signals and control recovery issues on the Homocysteine Enzymatic (HCYS) Assay can produce erroneous patient results (positive or negative bias)
Firm Action
Roche issued an URGENT MEDICAL DEVICE CORRECTION notice to its consignees on 10/17/2024 via UPS Ground. The notice explained the issue, clinical significance, and requested the following actions be taken:
"" HCYS kits lot number 747029 expired on September 30, 2024. Ensure any inventory you have of this lot has been discarded per your local guidelines.
" Follow your laboratory s standard operating procedures to determine specific clinical implications for your patients and whether retrospective review of patient results is required.
" Consult with the physician or pathologist at your facility to determine specific clinical implications for your patients.
" If your facility has distributed the affected product to another site, please ensure this UMDC is provided to that site."
For questions: contact the Roche Support Network Customer Support Center, 24 hours a day, seven days a week at 1-800-428-2336
Root Cause
Under Investigation by firm
Distribution Pattern
US: NJ, TX, NY, FL, IN, TX, OK, SC, IA,
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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