Olympus Scientific Solutions Americas Corporation — Class II medical device recall Z-0680-2017
Terminated recall by Olympus Scientific Solutions Americas, reported 2016-12-14, distributed in AZ, CA, CO, GA, IL, LA, MA, MD…. Possible unintentional x-ray emission after users attempt early termination of the sequence.
| Recall number | Z-0680-2017 |
|---|---|
| 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 | 2016-10-27 |
| Classified | 2016-12-07 |
| Reported by FDA | 2016-12-14 |
| Terminated | 2020-07-30 |
| Distributed | AZ, CA, CO, GA, IL, LA, MA, MD, MN, NJ, OH, PA, SC, TX, VA, WA |
| Quantity | 41 units |
Product
Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System
Reason for recall
Possible unintentional x-ray emission after users attempt early termination of the sequence.
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-0680-2017. 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.