Atellica IM CA 19-9 (50 Test)-In vitro diagnostic use in the quantitative measurement of the CA 19-9 tumor-associated antigen in human serum using the Atellica CI and Atellica IM Analyzers SMN: 10995490
FDA Recall Z-3100-2024 · Posted 2024-09-11
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Recalling FirmSiemens Healthcare Diagnostics, Inc.
Recall StatusOpen, Classified
Product CodeNIG
Date Initiated2024-07-26
Reason for Recall
Positive bias for some samples around the CA 19-9 upper limit of normal of 35 U/m as compared to the previous lot. The sample bias observed was greatest in the Asia Pacific sample population. The observed bias is not proportional across the assay measuring interval and is less pronounced for sample
results above a concentration of 110 U/mL.
Firm Action
Siemens has issued an Urgent Medical Device Correction (UMDC) AIMC 24-14.A.US to US customers, and an Urgent Field Safety Notice (UFSN) AIMC 24-14.A.OUS to Outside the US (OUS) customers on 7/26/24. Letter states reason for recall, health risk and action to take:
" Please review this letter with your Medical Director to determine the appropriate course of action, including for any previously generated results, if applicable.
" Perform the instructions provided below:
o Discontinue use of and discard the kit lots listed in the table above (Products
Section).
o If you experience this issue, you may request no-charge replacement product
from your local Siemens Healthineers or distributor office. Please review
your inventory of these products to determine your laboratory s replacement
needs and to provide information to Siemens Healthineers for reporting to
the authorities.
o Complete and return the Field Correction Effectiveness Check and indicate
product replacement needs on the form attached to this letter within 30
days.
o Please retain this letter with your laboratory records and forward this letter
to those who may have received this product.
Resolution CA 19-9 kit lots ending in 535 are not available for purchase or use. You may request no-charge replacement product from your local Siemens Healthineers or distributor office. If you have any questions, please contact your Siemens Healthineers Customer Care Center or your local Siemens Healthineers technical support representative.
Root Cause
Under Investigation by firm
Distribution Pattern
Worldwide - US Nationwide distribution
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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