Siemens Healthcare recalls Atel: 11099412 calibrators for in vitro diagnostics due to potential calibration errors in hsCRP tests. Affected units have specific lot numbers and expiration dates.
Atellica CH: The Atellica¿ CH High Sensitivity CReactive Protein Calibrator (hsCRP CAL) is for in vitro diagnostic use in calibrating the hsCRP assay using the Atellica¿ CH Analyzer.
Siemens Healthcare is recalling Atellica CH High Sensitivity C-Reactive Protein calibrators used with their analyzers. This recall is for potential calibration errors in blood tests that could affect test accuracy.
The calibrator is used to ensure accurate blood tests for inflammation markers. If not properly calibrated, test results could be inaccurate, potentially leading to incorrect health assessments.
Healthcare labs using Siemens Atellica CH calibrators for in vitro diagnostics are affected. Lab technicians and medical staff who handle these calibrators are most at risk.
Check for the Siemens Material Number (SMN) 11099412 on the calibrator. Affected units were sold with lot number 453716 and expire by January 28, 2020.
Look for the Siemens Material Number (SMN) 11099412 on the calibrator.
Siemens Healthcare is recalling Atellica CH High Sensitivity C-Reactive Protein calibrators used with their analyzers for potential calibration errors in blood tests.
Check for the Siemens Material Number (SMN) 11099412 on the calibrator. Affected units have lot number 453716 and expire by January 28, 2020.
The recall does not require immediate action; check the calibrator details to confirm if it is affected.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1261-2020 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-1261-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
