fda_device_problem_reports
Counts reports in the FDA MAUDE database for a device (generic type or brand name) by reported outcome: malfunction, injury, death or other. Gives journalists, litigation researchers and patients a quick sense of the reporting record for a device type, with the essential caveat attached. Source: FDA MAUDE medical device reports via openFDA. Counts are of reports, not confirmed incidents or causes, and cannot be used to rank how safe devices are; it does not return individual report narratives. (cost: 1 credit)
Tool call template
This tool declares no required parameters. Add optional parameters from the input schema as needed.
{
"id": 1,
"jsonrpc": "2.0",
"method": "tools/call",
"params": {
"arguments": {},
"name": "fda_device_problem_reports"
}
}Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| device | No | string, required, device generic name or brand name, e.g. "insulin pump" or "Omnipod" |