Olympus Scientific Solutions Americas Corporation — Class II medical device recall Z-2760-2017
Terminated recall by Olympus Scientific Solutions Americas, reported 2017-08-09, distributed nationwide. Instruments may, under certain specific circumstances listed below, fail to stop when a test is initiated and
| Recall number | Z-2760-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | FDA mandated |
| Recalling firm | Olympus Scientific Solutions Americas, Waltham, MA, United States |
| Recall initiated | 2017-07-11 |
| Classified | 2017-08-02 |
| Reported by FDA | 2017-08-09 |
| Terminated | 2023-05-03 |
| Distributed | Nationwide (US) |
| Quantity | 146 units |
Product
Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System, X-Ray Fluorescence
Reason for recall
Instruments may, under certain specific circumstances listed below, fail to stop when a test is initiated and no sample is present (proximity shut down fails to end test).
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-2760-2017. 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.