CELLSEARCH Circulating Tumor Cell Kit (Epithelial)-IVD intended for the enumeration of circulating tumor cells (CTC) of epithelial origin (CD45-, EpCAM+, and cytokeratins 8, 18+, and/or 19+) in whole blood Part Number: 7900001
FDA Recall Z-1345-2022 · Posted None
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Recalling FirmMenarini Silicon Biosystems
Recall StatusOpen, Classified
Product CodeNQI
Date Initiated2022-05-20
Product Quantity484 units
Reason for Recall
High number of total images/unassigned events including (dual positives) and the potential for false
positive results being placed into the image gallery in some patient samples
Firm Action
Menarini Silicon Biosystems issued notification telephone Urgent Medical Device Correction Notification CTC Kit Lot S108 to US on 5/20/22. Followed by e-mail direct to consignees for US sites - May 23, 2022 and Coordination with Asia Pacific region and the EU with Local QA and RA from the regions. Letter states reason for recall, health risk and action to take:
Discontinue usage of Lot S108 and quarantine the lot in your inventory for
disposal.
Review patient samples run with Kit Lot S108 which had results that were above
the cut-off. If you observe any images with the staining pattern of the false
positive images shown below or there is any uncertainty regarding these images
impacting the patient's outcome from below the cutoff to above the cut-off, the
patient sample should be repeated.
Report any previous occurrence of unusually high number of total images/
unassigned events or potential false positive events that have not already been
reported to the Customer Technical Support.
" Complete and return the enclosed Confirmation of Receipt form no later than May
31, 2022.
If you have additional questions about this issue, contact Customer Technical Support
at +1-877-837-4339 option 2
Root Cause
Process control
Distribution Pattern
CA FL IL IN MA MI NC NM NY OH ON PA TX Foreign: Italy, Shanghai, Singapore,
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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