RegPing FDA

RegPing FDA brings FDA regulatory activity straight into your team's Discord — so compliance and regulatory-affairs staff stay aware the moment something publishes, instead of refreshing FDA.gov.

What it monitors

• FDA recalls RSS for fast headline triggers


• openFDA device-recall, 510(k) clearance, and adverse-event (MAUDE) APIs for structured detail

Each new action is normalized, concisely summarized, and posted as a clean embed into the channel you choose. Recall alerts are enriched with classification (Class I/II/III), recalling firm, lot codes, and distribution scope.

Triage at a glance — every alert carries a plain-text severity label: urgent (Class I recalls, Death/Injury events), notice (Class II/III, notable clearances), info (routine items).

Filter to what you handle — use /filter by stream (recalls, clearances, adverse events), recall class, device class, adverse-event type, medical specialty, or minimum severity.

RegPing FDA is an awareness and monitoring tool. It surfaces and links the original FDA notice; it is not legal advice, compliance certification, or a substitute for reading the primary source. Billed as one per-server subscription through Discord — cancel anytime.