Siemens Healthcare Diagnostics Recalls

4 recalls found for Siemens Healthcare Diagnostics. Check if any of your products are affected.

HIGH
FDA DEVICE

epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System; Siemens Material Number (SMN): 10736515;

Use of the affected product can result in discrepant low pH and measured Total Carbon Dioxide (mTCO2) results and corresponding calculated values in arterial, venous, and capillary patient samples. An erroneously low pH or mTCO2 reading can lead to inappropriate treatment of nonexistent acidosis (respiratory of metabolic) or missed diagnosis of alkalosis (a true high pH: respiratory or metabolic alkalosis), potentially causing harm through unnecessary interventions with the former or failure to deliver appropriate treatment with the latter.

Siemens Healthcare Diagnostics
Use of
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HIGH
FDA DEVICE

Dimension Creatinine Flex reagent cartridge. Material Number: 10872079.

Siemens Healthcare Diagnostics is recalling certain lots of Dimension Creatinine Flex reagent cartridge (Dimension CRE2) because a potential imprecision in the Dimension CRE2 quality control (QC) and patient sample results using lot numbers GA6307 and BA7005 on the Dimension System. This imprecision may lead to erroneously decreased or increased creatinine patient results

Siemens Healthcare Diagnostics
Siemens Healthcare
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Healthcare Diagnostics Atellica CH A1c_E Recall for 21,291 Units (2026)

Siemens Healthcare Diagnostics recalled 21,291 Atellica CH A1c_E units distributed to laboratories nationwide and internationally in 2026. The recall addresses a depressed result bias when A1c_E is processed with RCRP on the same analyzer. Labs using separate analyzers are not impacted. Stop using the affected module immediately and follow manufacturer instructions. Contact Siemens or your lab’s F

Siemens Healthcare Diagnostics
A potential
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Health & Personal Care
HIGH
FDA DEVICE

Siemens Healthcare Diagnostics Recalls 4,885 Atellica CH Urine Albumin Tests for False Low Results (

Siemens Healthcare Diagnostics recalled 4,885 Atellica CH Urine Albumin tests in 2026 after detecting falsely depressed results. The manufacturer notes that any urine albumin concentration above 40.0 mg/dL may report values from 6.2 to 40.0 mg/dL. Stop using the device immediately and follow the recall instructions.

Siemens Healthcare Diagnostics
Falsely depressed
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