FDA Device recall Z-0680-2017
Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System
- FDA Device
- Class II
- terminated
- Published 2016-12-14
On 2016-12-14 the FDA classified a Class II recall of Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System by Olympus Scientific Solutions Americas, citing possible unintentional x-ray emission after users attempt early termination of the sequence.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0680-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-10-27 |
| Published | 2016-12-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Olympus Scientific Solutions Americas |
| Distribution | AZ, CA, CO, GA, IL, LA, MA, MD, MN, NJ, OH, PA, SC, TX, VA, WA |
Product
Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System
Reason
Possible unintentional x-ray emission after users attempt early termination of the sequence.
Identifiers
| code_info | Model - Vanta VCR |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0680-2017%22
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