Public recall detail

Atellica® CH Urine Albumin (UAlb)

2026-07-17

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Health products Health product recall
Quick summary

Quick summary: Atellica® CH Urine Albumin (UAlb). Reason: Health product recall. Category: Health products. Date: 2026-07-17.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: Atellica® CH Urine Albumin (UAlb). Reason: Health product recall. Category: Health products. Date: 2026-07-17.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandSiemens Healthcare Diagnostics Inc.
ProductAtellica® CH Urine Albumin (UAlb)
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82353

Affected products

ProductAtellica® CH Urine Albumin (UAlb)
LotMore than 10 numbers, contact manufacturer.
Model11537225
Serial numberMore than 10 numbers, contact manufacturer.
DescriptionAtellica® CH Urine Albumin (UAlb)

Issue

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 failuresThese issues may impact quality control (QC), calibrators, and patient results for the UN_c and A1c_E assays across all sample types.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Chemistry
CompaniesSiemens Healthcare Diagnostics Inc.511 Benedict Ave, Tarrytown, New York, United States, 10591
Recall date2026-07-09
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82353
Background{}
CompaniesSiemens Healthcare Diagnostics Inc.511 Benedict Ave, Tarrytown, New York, United States, 10591
AudiencesHealthcare
Source updated2026-07-17

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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