Siemens Healthcare recalls ADVIA 2120i Dual Aspirate Autosampler software versions 6.10 and 6.11 due to potential sample identification mismatches with 14-character barcodes. Affected units may require software update to prevent errors.
Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Siemens Healthcare is recalling specific software versions of the ADVIA 2120i Dual Aspirate Autosampler to prevent sample identification mismatches with 14-character barcodes. This could lead to incorrect lab results if the software misreads barcode labels on test samples.
The software may misread 14-character barcodes on test samples, causing incorrect sample identification. This could lead to wrong lab results but does not cause physical harm to users.
Lab technicians and healthcare facilities using the ADVIA 2120i Dual Aspirate Autosampler with software versions 6.10 or 6.11 are most at risk. The recall affects units sold in the U.S. between specific dates.
Check if your ADVIA 2120i Dual Aspirate Autosampler has software versions 6.10 or 6.11. The unique device identifier (UDI) is 00630414560045 for affected units.
Verify your autosampler's software version by checking the device settings or documentation.
The software may misread 14-character barcodes on test samples, leading to incorrect sample identification and potential lab result errors.
No, the recall does not require immediate discontinuation. Affected units can continue use after updating the software.
Check for software versions 6.10 or 6.11 on your ADVIA 2120i Dual Aspirate Autosampler. The unique device identifier (UDI) is 00630414560045 for affected units.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1391-2021 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-1391-2021 from Siemens Healthcare. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
