Fda Device Recalls Monitor
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Alexander Abernathy
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OpenFDA Device Recalls Monitor
Fetch medical device recall and enforcement data from OpenFDA.
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Retrieves medical device recalls, safety alerts, and enforcement actions from the FDA's OpenFDA device database.
Input
| Field | Type | Required | Default | Description |
|---|---|---|---|---|
queries | string[] | Yes | - | Medical device search queries |
maxItemsPerQuery | integer | No | 100 | Max records per query (1-1000) |
includeRaw | boolean | No | false | Include raw payload in output |
Example Queries
"pacemaker recall"- Pacemaker or cardiac implant recalls"infusion pump"- Specific device category search"defibrillator safety alert"- Device-safety-focused query
Output
| Field | Type | Description |
|---|---|---|
source | string | Always openfda_device |
query | string | Original search query |
recordType | string | device_recall or error |
title | string | Device/product name |
identifier | string | FDA report/code number |
date | string | Recall date (YYYY-MM-DD when available) |
url | string | Link to FDA device safety page |
summary | string | Device defect, risk, recall action |
recallClass | string | Structured FDA device recall classification |
deviceType | string | Device/product code or category when available |
manufacturer | string | Recalling establishment when available |
Example input
{"queries": ["pacemaker recall", "defibrillator safety alert"],"maxItemsPerQuery": 50,"includeRaw": false}
Example output
[{"source": "openfda_device","query": "pacemaker recall","recordType": "device_recall","title": "Cardiac Pacemaker Model XYZ","identifier": "Z-5678-2024","date": "2024-03-01","url": "https://www.fda.gov/medical-devices/medical-device-safety/recalls-device-technology","summary": "Recall: Z-5678-2024 | Classification: Class II | Establishment: MedDevice Corp | Reason: Battery depletion detected | Status: Ongoing","recallClass": "Class II","deviceType": "D12345","manufacturer": "MedDevice Corp"}]
Notes
- Data sourced from the OpenFDA public API.
- Device-focused queries now try to preserve the persona's intent instead of returning the same generic recall pool every time.
- Check https://www.fda.gov/medical-devices/medical-device-safety/recalls-device-technology for official device recall context.
Version: 0.2.0
Author: OpenClaw/Apify