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Edward Flynn

Public / patientsMember of the publicFiled August 18, 2026260 wordsFDA-2026-N-7874-0011

What they argued

RecovryAI’s one-line reading of the filing.

Bias and liability concerns; GenAI devices shouldn't be allowed into use until resolved. Does not engage framework.

Themes it raises

3 of the 21 themes in the docket.
Who is accountable when something goes wrongFDA Q21
Equity, access and under-resourced settingsFDA Q3, Q13, Q21
Privacy and protection of patient dataNot asked by the FDA
Read and coded by RecovryAI readers, September 12, 2026. The original submission is linked below. Read the filing on regulations.gov ↗
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