FDA recall record

Ortho-Clinical Diagnostics VITROS XT 3400 Chemistry System Product Code 6844458 Running recall — FDA Z-0546-2024

During planned monitoring of data post-release of Software Version 3.8.0 an increased occurrence of software issues relating to unresponsive subsystems,…

Class IIclassification
Z-0546-2024official record ID
Dec 20, 2023report date

Recall record at a glance

Official recordZ-0546-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOrtho-Clinical Diagnostics, Inc.
Report dateDec 20, 2023
Recall initiation dateOct 10, 2023
Quantity51 units
LocationRochester, NY, United States

Official product description

VITROS XT 3400 Chemistry System Product Code 6844458 Running Software Version 3.8.0

Why the product was recalled

During planned monitoring of data post-release of Software Version 3.8.0 an increased occurrence of software issues relating to unresponsive subsystems, unresponsive user interface (sometimes referred to as a screen freeze), and/or printer disconnections was identified. The consequence of these issues would be a delay in reporting results due to the required system shutdowns to recover the system. This delay in reporting results could occur during any assay, including which the speed of the result is deemed critical or STAT and could result in a delay of treatment in a patient. Due to the release strategy of this software version, the user could not update the system but a field engineer had to manually install each affected system.

Distribution information

US Nationwide. Global Distribution.

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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