Official recall record
Atellica® CH Urine Albumin (UAlb)
- Issuing authority
- Health Canada
- Alert date
- 2026-07-17
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Siemens Healthineers has confirmed, through the investigation of customer complaints, the potential for the following issues associated with processing Atellica CH Urine Albumin (UAlb) tests on Atellica CH and Atellica CI analyzers. • Falsely depressed Atellica CH Urea Nitrogen (UN_c) results • Falsely depressed Atellica CH Enzymatic Hemoglobin A1c (A1c_E) results • Increased rate of reaction cuvette QC failures These issues may impact quality control (QC), calibrators, and patient results for the UN_c and A1c_E assays across all sample types.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-07-28.