Official recall record
VITROS XT 7600 Integrated System Product Code 6844461 Running Software Version 3.8.0
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2023-10-10
- Country of alert
- United States
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 10758750031610
- Brand on record
- Ortho-Clinical Diagnostics, Inc.
- Product category
- Medical Device
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Record last checked against the registry on 2026-05-31.
Same barcode in other registries
The same EAN appears in 6 other official recall record(s) — a cross-border signal worth checking if you bought this product abroad.
- 2023-03-10 · US FDA — Medical Devices
VITROS XT 7600 Integrated System - For use in the in vitro quantitative, semi-quantitative, and qualitative measurement - 2024-01-26 · US FDA — Medical Devices
VITROS XT 7600 Integrated System, Catalog No. 6844461 - 2022-07-19 · US FDA — Medical Devices
VITROS XT 7600 Integrated System with Version 3.7.2 and below Product Code: 6844461 - 2024-01-22 · US FDA — Medical Devices
VITROS XT7600 Integrated System - 2024-01-26 · US FDA — Medical Devices
VITROS XT 7600 Integrated System, Catalog No. 6844461
Other recalls from this brand
- 2025-07-29 · US FDA — Medical Devices
VITROS Chemistry Products LAC Slides. Catalog Number: 8150112. 1 Sales Unit = contains 5 cartridges of 18 slid - 2025-06-12 · US FDA — Medical Devices
VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 1997. The VITROS OP Reagent is a dual-chambered - 2025-06-10 · US FDA — Medical Devices
Brand Name: VITROS Chemistry Products Product Name: VITROS Chemistry Products Performance Verifier II Model/
All 19 official recall notices naming Ortho-Clinical Diagnostics, Inc. on this site →