DATA INNOVATIONS, LLC
4 recall(s) on record — most severe on record: Class II.
Activity by year
- Recalls (4)
- Inspections (1)
Devices registered here (1)
- Blood Establishment Computer Software And AccessoriesProduct code MMH (opens in a new tab) · Class II · Hematology · 21 CFR 864.9165
Recalls & enforcement
- Class IITerminated2018-08-29Quality 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…
- Class IITerminated2014-10-23Software issue resulting in the results of one patient potentially being associated with another.
- Class IITerminated2014-08-15Potential issues with the ProVue driver have been identified which may cause data to be misassociated with patient results under a given set of circumstances.
- Class IITerminated2013-11-06When connected to the Sysmex UF-100, the Instrument Manager driver sysu100i driver software versions 7.00.0001, 7.00.0002, 7.00.0003, 7.00.0004, 7.00.0005, 8.00.0001, 8.00.0002, 8.00.0003, and 8.00.0004, and is configured with option "Strip Zeros from Result" set to "Yes" may …
FDA inspections (1)
- VAI2016-09-01Voluntary Action Indicated · Compliance: Devices · citations posted
Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.
Related
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)
Cite this record
RegWarden. “DATA INNOVATIONS, LLC (FEI 3001451449) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3001451449-data-innovations-llc/
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