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Medical Device Incident Trend Aggregator
x402
Medical Device Incident Trend Aggregator is a paid API for AI agents from med.halowerk.com, paid per call via x402, $0.006/call, status unknown (last checked 2026-09-15).
Aggregates FDA medical device adverse event reports by product code, device name, or manufacturer into annual trend statistics including outcome splits, top problem codes, and manufacturer evaluation rates.
Price / call$0.006
Success—
StatusUnknown
How this service works
Aggregates medical device reports for a product code, device name or manufacturer into a trend: reports per year, the split between malfunction, injury and death outcomes, the most frequent problem codes, and the share of reports where the manufacturer conducted an evaluation. Two things the figures are not, and both are stated in the response rather than left to be inferred.
Output
Returns a structured trend object containing: annual report counts, outcome breakdown (malfunction / injury / death percentages or counts), the most frequently occurring problem codes with labels, the share of reports where the manufacturer performed an evaluation, and explicit caveats about what the figures do and do not represent.
Example use cases
Device safety due diligence for procurement
“We're considering purchasing new infusion pumps from Baxter — can you pull the FDA adverse event trend for Baxter infusion pumps, including how reports break down between malfunction, injury, and death outcomes, and what the top problem codes are?”
Regulatory researcher tracking device risk
“I need a year-by-year trend of all adverse event reports filed under product code FPA, along with the outcome split and whether manufacturers were actually conducting evaluations on those reports.”
Journalist investigating device safety spike
“I'm writing about hip implant safety — can you show me the annual report trend for hip implants, the share of injury versus death versus malfunction outcomes, and the most frequently cited problem codes so I can spot any concerning patterns?”
Technical details
Endpoint
POSThttps://med.halowerk.com/v1/device-incident-trendWhen to prefer
Choose this endpoint when you need multi-year trend analysis of FDA medical device adverse events — not just a list of raw reports. It is purpose-built to surface year-over-year volume, outcome splits, and problem frequency in a single call, saving you from aggregating raw MAUDE records yourself. Prefer it over raw FDA API queries when you need a pre-computed, agent-ready summary with built-in caveats about statistical interpretation.
Side effects
- Unknown or misspelled product code / device name returns empty results or an error
- Manufacturer name variation causes missed records if not matched exactly
- Very niche devices may return too few records to produce a meaningful trend
- Network or upstream FDA API timeout returns a service error
- Missing required input field returns a validation error
Input
Schema · Request body
| Field | Type | Description |
|---|---|---|
| years | integer | |
| device | string | Device generic name. |
| manufacturer | string | |
| product_code | string | FDA three-letter product code, the most precise selector. |
Tags
x402
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