Siemens Healthcare recalls Atel: 11537222; UDI: 00630414610955 All Lots. Reagent carryover from other tests may cause inaccurate magnesium results. Contact for remedy.
Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP), Triglycerides (Trig), and Triglycerides_2 (Trig_2) Impacting Magnesium (Mg) Results
Siemens Healthcare is recalling Atellica CH Triglycerides_2 test kits because reagent carryover from other tests can lead to inaccurate magnesium results. This affects lab tests using the Atellica CH Analyzer. The recall covers all lots with serial number 11537222 and unique device identifier 00630414610955.
Reagent carryover from other tests (LDL Cholesterol Direct, Total Protein II, Triglycerides, and Triglycerides_2) can contaminate the magnesium test results. This may cause inaccurate magnesium measurements in lab samples.
Lab users who perform triglycerides tests with the Atellica CH Analyzer may be affected. Those using the specific test kits with serial number 11537222 or unique device identifier 00630414610955 are most at risk.
Check for the serial number 11537222 or unique device identifier 00630414610955 on the Atellica CH Triglycerides_2 test kits. These kits are used with the Atellica CH Analyzer for triglyceride testing in human serum and plasma.
Look for the serial number 11537222 or unique device identifier 00630414610955 on the Atellica CH Triglycerides_2 test kits.
The recall is due to reagent carryover from other tests (LDL Cholesterol Direct, Total Protein II, Triglycerides, and Triglycerides_2) impacting magnesium test results.
Inaccurate magnesium results may occur if reagent carryover from other tests contaminates the test kit.
Check for the serial number 11537222 or unique device identifier 00630414610955 on the Atellica CH Triglycerides_2 test kits.
We’ve drafted a message you can send Siemens Healthcare to request your refund or repair — edit it as you like.
Subject: Recall Z-1271-2023 — Siemens Healthcare Siemens Healthcare Hello, I own a Siemens Healthcare that is covered by recall Z-1271-2023 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.
