Data Foundry

Medical device recalls 2025

Brand Name: VITROS Product Name: VITROS 4600 Chemistry System… — Class II medical device recall Z-2040-2025

Ongoing recall by Ortho-Clinical Diagnostics, Inc., reported 2025-07-09, distributed nationwide. a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the s

Recall numberZ-2040-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmOrtho-Clinical Diagnostics, Inc., Rochester, NY, United States
Recall initiated2025-05-09
Classified2025-06-27
Reported by FDA2025-07-09
DistributedNationwide (US)
Countries outside the USAU, BE, BM, BR, CA, CL, CN, CO, DE, DK, ES, FR, GB, IN, IT, JP, MX, NL, NO, PT, RU, SE, SG
Reason classessoftware
UPC / GTIN / UDI-DI10758750012343, 10758750033201
Serial numbers46000111-46001897
Model numbers6802445, 6900440

Product

Brand Name: VITROS Product Name: VITROS 4600 Chemistry System Model/Catalog Number: (1) 6802445, (2) 6900440 Software Version: version 3.2 to version 3.8.3 (all available software versions) Product Description: In vitro diagnostic chemistry analyzer.

Reason for recall

a software anomaly allows test results to be reported using Micro Tip and Micro Slide diluent packs that the system treats as expired even when the Use Expired Reagents setting is not enabled if a shelf expiration date is omitted during manual loading. The issue was identified by a customer complaint, in which a CREA Urine test was processed with an RE (Reagent Expired) code, even though the diluent pack was not expired and the use-expired-reagents setting was disabled. This can result in erroneous test results and/or delaying test results.

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-2040-2025. 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.