FDA recall record

Ortho-Clinical Diagnostics VITROS XT 3400 Chemistry System with Version 3.7.2 and below recall — FDA Z-1675-2022

Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems may cause a positive or negative shift in the electrical current supplied to the…

Class IIclassification
Z-1675-2022official record ID
Sep 14, 2022report date

Recall record at a glance

Official recordZ-1675-2022
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOrtho-Clinical Diagnostics, Inc.
Report dateSep 14, 2022
Recall initiation dateJul 19, 2022
Quantity506 units
LocationRochester, NY, United States

Official product description

VITROS XT 3400 Chemistry System with Version 3.7.2 and below Product Code: 6844458

Why the product was recalled

Performing a system shutdown on VITROS XT 3400 and VITROS XT 7600 Systems may cause a positive or negative shift in the electrical current supplied to the LED used in conjunction with the Digital Imaging Reflectometer. Potential exists for either a positive or negative shift in results reported by the VITROS System.

Distribution information

Worldwide distribution - US Nationwide and the countries of Australia, Belgium, Bermuda DV04, Brazil, Canada L3R 4G5 , Chile, China, Colombia, Denmark, France, France, Germany, India, Italy, Japan, Mexico, Norway, Portugal, Russia, Singapore 609917, Spain, Sweden, The Netherlands, United Kingdom.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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