Public recall detail

Atellica CH Enzymatic Hemoglobin A1c (A1c_E) assay

2026-06-18

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Health products Health product recall
Quick summary

Quick summary: Atellica CH Enzymatic Hemoglobin A1c (A1c_E) assay. Reason: Health product recall. Category: Health products. Date: 2026-06-18.

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 Enzymatic Hemoglobin A1c (A1c_E) assay. Reason: Health product recall. Category: Health products. Date: 2026-06-18.

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 Enzymatic Hemoglobin A1c (A1c_E) assay
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82220

Affected products

ProductAtellica CH Enzymatic Hemoglobin A1c (A1c_E) assay
LotAll lots.
Model11097536
Serial numberAll lots.
DescriptionAtellica CH Enzymatic Hemoglobin A1c (A1c_E) assay

Issue

Siemens Healthineers has confirmed, through internal investigation of customer complaints, the potential for intermittent well-to-well bias affecting the A1c_E/A1c_H assay when used on the Atellica CH and Atellica CI systems. This observed bias does not affect every A1c_E reagent lot or reagent pack. However, affected wells cannot currently be identified prospectively, therefore all in-date lots are considered potentially impacted until further notice. Under certain circumstances, this issue may result in:. Falsely depressed patient results when lot calibration is performed using an affected well and patient testing is subsequently performed using an unaffected well.. Falsely elevated patient results when lot calibration is performed using an unaffected well and patient testing is subsequently performed using an affected well.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Medical devices - Chemistry
CompaniesSiemens Healthcare Diagnostics Inc.511 Benedict Ave, Tarrytown, New York, United States, 10591
Recall date2026-06-10
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82220
Background{}
CompaniesSiemens Healthcare Diagnostics Inc.511 Benedict Ave, Tarrytown, New York, United States, 10591
AudiencesGeneral public Healthcare Industry
Source updated2026-06-18

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

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