Public recall detail

VITROS Immunodiagnostic Products Anti-HBs Calibrators And Reagent

2024-05-30

medium
Recall Safety notice
Quick summary

Quick summary: VITROS Immunodiagnostic Products Anti-HBs Calibrators And Reagent. Date: 2024-05-30.

Recommended action

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

Recall details

Quick summary: VITROS Immunodiagnostic Products Anti-HBs Calibrators And Reagent. Date: 2024-05-30.

Official details

Affected product details

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

BrandOrtho-Clinical Diagnostics
ProductVITROS Immunodiagnostic Products Anti-HBs Calibrators And Reagent
IssueMedical devices - Performance
Recall classType II
IdentificationRA-75591

Affected products

ProductVITROS Immunodiagnostic Products Anti-HBs Calibrators And Reagent
Lot5111 5120
Model152 4693 178 7753
Serial number5111 5120
DescriptionVITROS Immunodiagnostic Products Anti-HBs Calibrators And Reagent

Issue

QuidelOrtho's internal stability testing of VITROS anti-HBs calibrators detected a gradual reduction in calibration signal for calibrator levels 2 and 3 over the shelf life of the product for the specified lots. This reduction in signal may affect the shape of the calibration curve generated during calibration, compared to the calibration curve generated earlier in the product's shelf life. A change in the shape of the calibration curve may cause patient and QC samples tested using the associated VITROS® immunodiagnostic products anti-HBs reagent pack to report results as falsely elevated, potentially causing negative results to report as borderline, and borderline results to report as positive. This issue is detectable by performing QC as results generated will be higher than expected and/or outside the expected limits for QC, depending on the age of the lot and amount of signal reduction experienced in calibrator levels 2 and 3. Recall start date: May 21, 2024

What you should do

  • Contact the manufacturer if you require additional information.
Additional official information
AudienceHealthcare
CategoryHealth products - Medical devices - Immunology
CompaniesOrtho-Clinical Diagnostics Felindre Meadows, Bridgend, Great Britain, CF35 5PZ
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-75591
Background{}
CompaniesOrtho-Clinical Diagnostics Felindre Meadows, Bridgend, Great Britain, CF35 5PZ
AudiencesHealthcare
Source updated2024-05-30

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

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