Recall Z-0803-2016— Olympus Scientific Solutions Americas
Class II · Terminated
Class II FDA medical device recall by Olympus Scientific Solutions Americas, initiated 2016-01-13, terminated 2021-05-18. FDA's recall record names no specific 510(k) clearance for this event. Product: Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF Analyzer . This is a Analytical X-ray system. Reason: The Firm has discovered a Software bug..
- Recalling firm
- Olympus Scientific Solutions Americas
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-01-13
- Terminated
- 2021-05-18
- Firm location
- Waltham, MA, United States
Product description
Olympus Scientific Solutions Americas Corporation ( OSSA ) Delta XRF Analyzer . This is a Analytical X-ray system
Reason for recall
The Firm has discovered a Software bug.
Data sourced from openFDA. This site is unofficial and independent of the FDA.