ADVIA Centaur aTPO Assay, Material Number 10630886 (100 Test) and 10630887 (500 Test)
FDA Recall Z-3304-2024 · Posted 2024-09-27
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Recalling FirmSiemens Healthcare Diagnostics, Inc.
Recall StatusOpen, Classified
Product CodeJZO
Date Initiated2024-08-21
Product Quantity5622 kits
Reason for Recall
Positive bias in patient results at and below the cut-off of 60 U/mL with the lots listed in the table below when compared to alternate lots on the Atellica IM analyzer.
Firm Action
An Urgent Medical Device Correction notification letter dated 8/21/24 was sent to customers.
Customer Actions
" 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 actions provided below:
o Discontinue use of and discard the kit lots listed in the table above (Products Section).
o 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.
You may request no-charge replacement product from your local Siemens Healthineers or distributor office.
Unaffected reagent lots are available for ordering.
Please send a scanned copy of the completed form via email to: [email protected]
Or to fax this completed form to the Customer Care Center at: (312) 275-7795
We apologize for the inconvenience this situation may cause. 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 distribution - US Nationwide.
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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