Data Innovations, Llc
463 Mountain View Dr Ste 305, Colchester, VT, US
Registered product codes
3 product codes
Recent MDR events
96 on file
- Instrument Manager SoftwareJul 27, 2026Other1225673-2026-00010
- INSTRUMENT MANAGER SOFTWAREJul 10, 2026Malfunction1225673-2026-00009
- INSTRUMENT MANAGER SOFTWAREJul 2, 2026Malfunction1225673-2026-00008
- INSTRUMENT MANAGER SOFTWAREMay 31, 2026Malfunction1225673-2026-00006
- INSTRUMENT MANAGER SOFTWAREApr 22, 2026Malfunction1225673-2026-00005
- INSTRUMENT MANAGER SOFTWAREMar 6, 2026Malfunction1225673-2026-00004
- INSTRUMENT MANAGERFeb 18, 2026Malfunction1225673-2026-00003
- INSTRUMENT MANAGER SOFTWAREFeb 11, 2026Malfunction1225673-2026-00002
- INSTRUMENT MANAGER SOFTWAREJan 21, 2026Malfunction1225673-2026-00001
- INSTRUMENT MANAGER SOFTWARENov 25, 2025Malfunction1225673-2025-00007
Recalls
3 on file
- TerminatedFeb 16, 2017
Software issue resulting in the results of one patient potentially being associated with another.
View FDA record ↗ - TerminatedSep 12, 2014
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.
View FDA record ↗ - TerminatedUnknown
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 results from a quality control (QC) sample ID ("Q^Control" in SPM segment), and the option Hold Results Until Complete is enabled, the results do not parse into IM. The communication Trace shows the sample being transmitted, but no information is logged in the Specimen Event Log (SEL). There is a potential for harm if QC results are not processed, downstream auto verification rules may misfire based on missing QC results leading to a delay in, or incorrect treatment. QC results will not be available for evaluation by the lab. There have been no reported instances of patient harm from this malfunction.
View FDA record ↗
Compliance history
Matched by FEI 3001451449.
FDA inspections
0 on file
No inspections on file for this FEI number.
Inspection citations
0 on file
No citations on file for this FEI number.
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.