Medical Device Recall Death Triangle — Region Gauge is a paid API for AI agents from aeml-x402.zeabur.app, paid per call via x402, $0.25/call, status unknown (last checked 2026-09-13).
Aggregates FDA/EUDAMED device authorization lifecycle, MAUDE adverse event surges, and FDA recall classification cascades for a given medical device product line into a single cross-validated risk gauge.
[3-LEG] Medical device recall chain, one product line (?entity=philips-dreamstation-cpap): leading recall pressure signals -> current current clearance status -> realized lifecycle from cleared to recalled to withdrawn (confirmation gate). A sequential chain, not one reading - confidence = how many legs are lit, in order. Sources: US FDA. Descriptive only, never a forecast or advice. No data -> 422 no_charge, not billed.
Returns a structured gauge object with named legs covering: device authorization lifecycle (cleared/recall/withdrawn/revoked), MAUDE adverse event current surge and severity, and FDA recall classification cascade. Also includes a cross-line narrative description, provenance with data lineage and freshness indicators, Ed25519-signed citations traceable to openFDA/EUDAMED, decision points for re-runs with alternate entity tags, and honest scope/grade disclosures. Data is screening-level, not decision-grade.
GEThttps://aeml-x402.zeabur.app/gauge/meddevice-regionChoose this endpoint when you need a multi-signal, cross-validated medical device risk snapshot combining regulatory lifecycle, adverse event early-warning, and recall-cascade downstream signals in a single call. Prefer it over manually querying openFDA or EUDAMED separately when the use case is procurement due diligence, hospital supply chain risk, or investment screening on a specific device product line. Not suitable for real-time clinical decision support or legal advice.
| Field | Type | Description |
|---|---|---|
| input | object | |
| output | object |
{
"type": "json"
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