HomeMedical Device recalls
Medium severity

Atellica CH Urine Albumin (UAlb). Material Number: 11537225

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateJanuary 20, 2026
ReportedMarch 11, 2026
Recalling firmSiemens Healthcare Diagnostics, Inc.
Country / regionUnited States NY

Hazard

Falsely depressed UAlb patient results may occur. Affected samples with any urine albumin concentration above the UAlb measuring interval >40.0 mg/dL may report values between 6.2 mg/dL and 40.0 mg/dL.

Affected products

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