Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field., part of Olympus CorporationLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Olympus Scientific Solutions Americas with 6 device recalls. The most recent is a device recall dated Jul 11, 2017: Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Jul 11, 2017 | Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray System, X-Ray FluorescenceClass II · Instruments may, under certain specific circumstances listed below, fail to stop when a test is initiated and no sample | Device recalls |
| Jan 7, 2017 | Olympus Scientific Solutions Americas Corporation ( OSSA ) VANTA¿ XRF Analyzer. Model Vanta VCR and Vanta VMR Analytical X-ray systemsClass II · It was discovered under rare circumstances the LED warning light circuit could fail. If this happens, while the instrume | Device recalls |
| Oct 27, 2016 | Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: VANTA Analytical X-Ray SystemClass II · Possible unintentional x-ray emission after users attempt early termination of the sequence. | Device recalls |
| Jun 22, 2016 | Olympus Scientific Solutions Americas Corporation ( OSSA ) Model: Analytical X-Ray System X -Ray Fluorescence. Intended to emit ionizingClass II · Trigger lock option does not always prevent x-ray generation. Specifically if the unit is in test mode or repeat test m | Device recalls |
| Jan 13, 2016 | Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF Analyzer . This is a Analytical X-ray systemClass II · The Firm has discovered a Software bug. | Device recalls |
| Jun 9, 2015 | Olympus Scientific Solutions Americas Analytical X-ray System. Delta, Delta Element, Delta Plus, DPO-4000-XX-U-EN-EN-PM-SP12, DPO-6000-XX-Class II · Higher than published scatter around the probe head when testing some samples. At the point the customer would interact | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
