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ForgeMesh Medical Device Recall Search
x402
ForgeMesh Medical Device Recall Search is a paid API for AI agents from x402.forgemesh.io, paid per call via x402, $0.01/call, status unknown (last checked 2026-09-14).
Searches official US FDA enforcement reports for recalled medical devices, returning severity class, defect reason, recalling firm, distribution scope, and key dates.
Price / call$0.01
Success—
StatusUnknown
How this service works
Medical device recall search over official US enforcement reports: category 'device' plus a keyword returns recalled devices with severity class, defect reason, firm, distribution, and dates. Class I entries flag reasonable probability of serious harm — surface those first.
Output
A JSON object containing a list of recalled medical device records (up to the requested limit), each with: recall number, product description, recalling firm, classification (Class I/II/III), reason for recall, distribution scope, recall initiation date, report date, and status. Also includes a note explaining classification severity levels, the echoed query parameters, a count of returned results, and an attribution line to US FDA public domain enforcement reports.
Example use cases
Patient safety device check
“Can you check the FDA recall database for any recalls on 'pacemaker' medical devices and flag any Class I entries since those indicate serious harm risk? Show me up to 15 results.”
Healthcare compliance audit
“Pull up the latest FDA enforcement reports for recalled 'infusion pump' devices — I need the recalling firm, defect reason, and distribution scope for each one. Give me up to 25 results.”
Medical product liability research
“Look up FDA device recalls related to 'hip implant' and return the most recent 10 — I need the recall classification, dates, and which firms initiated the recall.”
Technical details
Endpoint
POSThttps://x402.forgemesh.io/medical-device-recallsWhen to prefer
Choose this endpoint when you need structured, searchable access to US FDA medical device recall data with severity classification — especially when you need to surface Class I (serious harm risk) recalls first. Prefer this over generic web search when you need machine-readable, structured recall records including firm names, defect reasons, and distribution scope, directly from official FDA enforcement reports. Best for compliance checks, patient safety research, product liability investigation, and regulatory monitoring of the medical device category specifically.
Side effects
- No results returned if keyword matches no FDA enforcement records in the device category
- Invalid category value (not 'device') causes error or defaults to food
- Limit exceeds maximum of 25 and is rejected
- Empty query may return newest device recalls rather than keyword-filtered results
- Upstream FDA data latency may mean very recent recalls are not yet indexed
- Payment failure (insufficient USDC balance) blocks request at x402 layer
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| limit | integer | |
| query | string | product keyword, e.g. 'peanut' — empty returns newest in category |
| category | string | recall category (default food) |
Output
Schema · Response
{
"type": "json",
"example": {
"note": "classification: Class I = reasonable probability of serious harm; II = temporary/reversible harm; III = unlikely harm.",
"query": {
"query": "peanut",
"category": "food"
},
"recalls": [
{
"reason": "Potential Salmonella contamination",
"status": "Ongoing",
"report_date": "20260810",
"distribution": "Nationwide",
"recall_number": "F-1234-2026",
"classification": "Class I",
"recalling_firm": "Example Foods LLC",
"recall_initiated": "20260801",
"product_description": "Example Peanut Butter 16oz jars"
}
],
"returned": 3,
"attribution": "US FDA enforcement reports (public domain)"
}
}Tags
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