Data Foundry

Medical device recalls 2025

VITROS Chemistry Products OP Reagent Gen 15 — Class II medical device recall Z-2073-2025

Ongoing recall by Ortho-Clinical Diagnostics, Inc., reported 2025-07-09, distributed nationwide. Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may generate lower than expected quality

Recall numberZ-2073-2025
Product typeMedical device
ClassificationClass II
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmOrtho-Clinical Diagnostics, Inc., Rochester, NY, United States
Recall initiated2025-06-12
Classified2025-07-02
Reported by FDA2025-07-09
DistributedNationwide (US)
Countries outside the USAU, BE, BR, CA, CL, CN, CO, DE, DK, ES, FR, GB, IN, IT, JP, MX, NL, NO, PT, RU, SE, SG
Quantity2,017 units
UPC / GTIN / UDI-DI10758750001835
Lot numbers1527-15-2749
Model numbers1997, 680
Expiration dates2025-11-17, 2025-12-17, 2026-04-11, 2026-05-15

Product

VITROS Chemistry Products OP Reagent Gen 15. Model Number: 680 1997. The VITROS OP Reagent is a dual-chambered package containing ready-to-use liquid reagents that are used to detect opiates in urine. One sales unit contains 6 Microtip packs of reagent. Each pack has 50 OP tests.

Reason for recall

Lots from Generation (GEN) 15 of VITROS Chemistry Products OP Reagent may generate lower than expected quality control (QC) results. If the customer is unable to get passing quality control results, then the customer would be unable to run the OP-LO protocol leading to a potential delay in patient 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-2073-2025. 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.