Public recall detail

DCA Vantage® HbA1c (DX Claim)

2026-07-22

medium
Health products Health product recall
Quick summary

Quick summary: DCA Vantage® HbA1c (DX Claim). Reason: Health product recall. Category: Health products. Date: 2026-07-22.

Recommended action

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

Recall details

Quick summary: DCA Vantage® HbA1c (DX Claim). Reason: Health product recall. Category: Health products. Date: 2026-07-22.

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.
ProductDCA Vantage® HbA1c (DX Claim)
IssueMedical devices - Performance
Recall classType II
IdentificationRA-82378

Affected products

ProductDCA Vantage® HbA1c (DX Claim)
Lot0916065
Model10698915
Serial number0916065
DescriptionDCA Vantage® HbA1c (DX Claim)

Issue

Siemens Healthineers has confirmed through customer complaint investigation and internal testing that delamination of the buffer pull-tab may occur in a small subset of cartridges. Delamination occurs when bonded material layers within the pull-tab separate, preventing full release of the buffer solution into the reaction chamber and reducing the reagent volume available for analysis.When delamination occurs, it may result in falsely low (negatively biased) HbA1c results or instrument-generated error codes that prevent completion of the test. The issue observed in approximately 0.07-0.5% of cartridges in these lots. The majority of the cartridges in these lots continue to perform as intended.

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Medical devices - Haematology
CompaniesSiemens Healthcare Diagnostics Inc.511 Benedict Ave, Tarrytown, New York, United States, 10591
Recall date2026-07-13
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-82378
Background{}
CompaniesSiemens Healthcare Diagnostics Inc.511 Benedict Ave, Tarrytown, New York, United States, 10591
AudiencesGeneral public Healthcare Industry
Source updated2026-07-22

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

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