ProductGuru Recalls

Official recall record

Atellica® CH Urine Albumin (UAlb)

Health Canada · 2026-07-17 · CanadaType II
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.

Verify at the source: Health Canada — official record →
Record last checked against the registry on 2026-07-28.

More recalls: Health Canada · Canada · all filters

ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.