PlainRecalls
FDA Devices Moderate Class II Ongoing

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

Reported: December 20, 2023 Initiated: October 10, 2023 #Z-0546-2024

Product Description

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

Reason for Recall

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.

Details

Units Affected
51 units
Distribution
US Nationwide. Global Distribution.
Location
Rochester, NY

Frequently Asked Questions

What product was recalled?
VITROS XT 3400 Chemistry System Product Code 6844458 Running Software Version 3.8.0. Recalled by Ortho-Clinical Diagnostics, Inc.. Units affected: 51 units.
Why was this product 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.
Which agency issued this recall?
This recall was issued by the FDA Devices on December 20, 2023. Severity: Moderate. Recall number: Z-0546-2024.