fda
4 records
FDA Device Recall: IM Abbott Alinity ci-series (abdicqii) accessory driver v8.00.0001 software prod
2018-10-31
Class II — Quality control results are not processed for Abbott Diagnostics Alinity ci series (abdicqii) instrument. This has been determined to be a driver malfunction. When an instrument transmits ...
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FDA Device Recall: JResultNet drivers using ASTM coding language. Calculator/data processing modul
2017-04-05
Class II — Software issue resulting in the results of one patient potentially being associated with another.
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FDA Recall: Data Innovations, LLC — Class II
20140924
Potential issues with the ProVue driver have been identified which may cause data to be misassociated with patient results under a given set of circum | Product: ProVue Instrument Driver for JResultNe...
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FDA Device Recall: ProVue Instrument Driver for JResultNet (ProVue.jrm) v. 1.5.3 and below JResu
2014-09-24
Class II — Potential issues with the ProVue driver have been identified which may cause data to be misassociated with patient results under a given set of circumstances.
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ny_corps
1 records
NY Corp: DATA INNOVATIONS, LLC
2020-07-24
DOMESTIC LIMITED LIABILITY COMPANY | County: Tompkins | Jurisdiction: New York
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USASpending
2 records
Federal Award: DATA INNOVATIONS LLC — $2,235,534
2024-09-30
INSTRUMENT MANAGER PROFESSIONAL SOFTWARE AND IMPLEMENTATION SUPPORT FOR LABORATORY
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