ADVANCED INSTRUMENTS, LLC
2 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (2)
Registered facilities (2)
- Advanced Instruments, LLC FEI 1217058 · MA
- Advanced Instruments, LLC FEI 1221020 · ME
Recalls & enforcement
- Class IIOngoing2024-03-11System error messages may delay the ability to test patient samples and the need for frequent calibration due to results outside the expected range when testing controls.
- Class IITerminated2018-02-07RBC Reagent failure. High fluorescent counts during RBC Reagent + Diluent QC check that will result in failed QC check, preventing user from testing patient samples for RBC.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “ADVANCED INSTRUMENTS, LLC — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-1217058-advanced-instruments-llc/
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