Recall Z-0844-2019

Ortho Clinical Diagnostics Inc · initiated November 29, 2018

Class II Terminated

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Vitros Myoglobin Calibrators, Product Code 6801043 For use in the calibration of the VITROS ECi/ECiQ Immunodiagnostic Systems, the VITROS 3600 Immunodiagnostic System and the VITROS 5600 Integrated System for the quantitative measurement of myoglobin in human serum and plasma

Codes / lots: Lots 1271 through 1310 (expired) Lots 1315 & Above (in-date)

Reason for recall

A stability issue in the calibrators may cause calibration failures or atypical Quality Control results following a successful calibration.

FDA-determined cause: Under Investigation by firm

Action taken

On November 29, 2018, the firm sent a customer letter all affected customers. All consignees were notified of the issue and informed of revised instructions for VITROS Myoglobin Calibrators: - Reconstitute the calibrators using 1.0 mL distilled water, as per current instructions. - Allow reconstituted calibrator vials to stand at room temperature for 2 hours and then proceed with calibration within 2 hours (4 hours total) - Discard reconstituted calibrators after 4 hours. - Acknowledge the information contained in this notification by completing and submitting the Confirmation of Receipt form no later than December 14, 2018. - Post this notification by each VITROS System at your facility that processes this assay or with the user documentation. - Please forward this notification if the product was distributed outside of your facility. If you have questions, please contact Ortho Care Technical Solutions Center at 1-800-421-3311.

Details

Recall number
Z-0844-2019
Initiated
November 29, 2018
Terminated
February 6, 2024
Product code
JIS – Calibrator, Primary
Quantity
4030
Distribution
Distributed nationwide domestically. Foreign distribution to Australia, Brazil, Canada, Chile, China, Colombia, India, Japan, Mexico, Singapore, UK, France, Germany, Italy, Spain, Portugal, Poland, Russia, Denmark, Norway, Sweden, Belgium, and the Netherlands.
Recalling firm
Ortho Clinical Diagnostics Inc, Raritan, NJ

Official FDA recall record