ADVIA Chemistry Iron_2 (IRON_2) Reagents, Material Numbers 10377510 (6 x 350 tests) and 10341118 (7 x 145 tests)
FDA Recall Z-2666-2023 · Posted 2023-09-30
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Recalling FirmSiemens Healthcare Diagnostics, Inc.
Recall StatusOpen, Classified
Product CodeCDQ
Date Initiated2023-08-08
Product Quantity4966 reagents
Reason for Recall
There is a potential for a positive bias on Quality Control (QC) and patient sample results when using some IRON_2 reagent wedge pairs. When the issue occurs, the observed bias will vary wedge to wedge.
Firm Action
An Urgent Medical Device Correction notification letter dated 8/8/23 was sent to customers.
Actions to be Taken by the Customer
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 in Additional Information.
Complete and return the Field Correction Effectiveness Check Form attached to this letter within 30 days.
If you have received any complaints of illness or adverse events associated with the products listed in Table 1, immediately contact your local Siemens Healthineers Customer Care Center or your local Siemens Healthineers technical support representative.
Please retain this letter with your laboratory records and forward this letter to those who may have received this product.
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.
Additional Information
Please complete these instructions with each wedge set in your inventory prior to processing patient samples.
1. Ensure only one R1 and one R2 is onboard the system.
2. Run each level of QC that your laboratory has identified for use with IRON_2 on that reagent wedge set and determine if your QC criteria are met.
3. If acceptance criteria IS met, proceed using the R1/R2 wedge to generate patient results.
4. If the acceptance criteria IS NOT met, discard the reagent wedge set. If you have another set of IRON_2 reagent, repeat steps 1 3 and assess acceptance.
Root Cause
Under Investigation by firm
Distribution Pattern
US Nationwide. Global Distribution
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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