Data Foundry

Medical device recalls 2024

VITROS 4600 Chemistry System Catalog Nos — Class II medical device recall Z-1225-2024

Ongoing recall by Ortho-Clinical Diagnostics, Inc., reported 2024-03-13, distributed nationwide. A software defect affecting VITROS Systems running VITROS Software Versions 3.8.1 causes QC baseline statistic

Recall numberZ-1225-2024
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmOrtho-Clinical Diagnostics, Inc., Rochester, NY, United States
Recall initiated2024-01-26
Classified2024-03-01
Reported by FDA2024-03-13
DistributedNationwide (US)
Countries outside the USAU, BE, BR, CA, CN, CO, ES, FR, GB, IN, IT, MX, RU, SG
Reason classessoftware
UPC / GTIN / UDI-DI10758750012343, 10758750033201
Serial numbersJ46000150, J46000190, J46000240, J46000499, J46000564, J46000801, J46000821, J46000898, J46000910, J46000933, J46001029, J46001030, J46001041, J46001042, J46001186, J46001187, J46001210, J46001217, J46001289, J46001293, J46001639, J46001645
Model numbers6802445

Product

VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440 (refurbished)

Reason for recall

A software defect affecting VITROS Systems running VITROS Software Versions 3.8.1 causes QC baseline statistics to not update as expected when changed by the user. This may cause erroneous patient results to be reported.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1225-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.