# FDA device recall: Atellica CH Urine Albumin REF: 11537225, in vitro diagnostic

> recall · VERIFIED · 2026-07-06

Firm: Siemens Healthcare Diagnostics, Inc. · Class II · Processing of urine albumin assay on the CI analyzers may lead to the following issues: Falsely depressed Atellica CH Urea Nitrogen (UN_c) results; Falsely depressed Atellica CH Enzymatic Hemoglobin A

- Company: Siemens Healthcare Diagnostics, Inc.
- Sector: diagnostics
- Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Source: MedFuel Intel news monitor. Verification tier: VERIFIED. Informational only, not investment advice. Corrections: media@medfuelinc.com.