FDA Recall Open, Classified

VITROS Immunodiagnostic Products Anti-HBs Quantitative Reagent Pack, Catalog No. 6801925 VITROS Immunodiagnostic Products Anti-HBs Calibrators, Catalog No. 6801926

Recall: Z-0772-2024 · Initiated November 27, 2023

Recall

Recall Number
Z-0772-2024
Event Number
93632
Firm
Ortho-Clinical Diagnostics, Inc.
FEI Number
1000136573
Product Code
LOM
Status
Open, Classified
Root Cause
Nonconforming Material/Component
Initiated
November 27, 2023
Posted
January 19, 2024
Address
100 Indigo Creek Dr, Rochester, NY, 14626-5101

Description

VITROS Immunodiagnostic Products Anti-HBs Quantitative Reagent Pack, Catalog No. 6801925 VITROS Immunodiagnostic Products Anti-HBs Calibrators, Catalog No. 6801926

Reason

Affected lots may experience increased calibration failures or an increase in falsely elevated results.

Action

On 27 November 2023, consignees who had been shipped the affected VITROS Anti-HBs Reagent Pack and Calibrator were notified of the issue via Urgent Production Correction Notification letters. Customers were instructed to immediately discontinue using, render unusable, and discard all affected lots of the affected product from their inventory. - QuidelOrtho will provide credit or replacement for the discarded product. - QuidelOrtho recommends a review of previous results between 12-30 mIU/mL, which were generated using an affected lot of VITROS anti-HBs Reagent Pack, where only anti-HBs testing was performed and was positive (for example, postvaccination testing) or where only anti-HBs was positive in the triple-panel test. If you have further questions, please contact QuidelOrtho's Global Services Organization (formerly Ortho Care) at 1-800-421-3311.

Distribution

Domestic distribution nationwide. OUS distribution to Bermuda, Australia, Brazil, Canada, Chile, China, Columbia, India, Japan, Mexico, Singapore, UK, France, Germany, Italy, Spain, Portugal, Russia, Denmark, Norway, Sweden, France, Belgium, and The Netherlands.

Quantity

6,920 US; 57 OUS