FDA Medical Device Recall Scraper
Pricing
$5.00 / 1,000 results
FDA Medical Device Recall Scraper
Fetch FDA medical device recall records via OpenFDA. Filter by device name and date. Returns recall number, reason, risk class, company and recall status.
Pricing
$5.00 / 1,000 results
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Developer
azureblue
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2
Total users
1
Monthly active users
2 days ago
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Retrieve FDA medical device recall records from OpenFDA. Filter by device name and date range. Returns recall number, reason for recall, risk classification, company, recall status and direct FDA links.
Features
- Searches FDA's full device recall database (100,000+ records)
- Filter by product description keyword and initiation date
- Handles 429 rate limiting automatically (10s backoff)
- OpenFDA error handling (returns clean "no results" instead of crashing)
- Pagination via
skipparameter — up to 10,000 records per run - No API key required
Input
| Field | Type | Required | Default | Description |
|---|---|---|---|---|
deviceName | string | — | Device keyword, e.g. pacemaker or insulin pump | |
dateFrom | string | — | Filter from date, format YYYY-MM-DD | |
country | string | US | Country code (OpenFDA covers US) | |
maxResults | integer | 50 | Max records (1–10,000) |
Leave deviceName empty to retrieve the most recent recalls across all devices.
Output
{"recallNumber": "Z-0001-2024","deviceName": "IMPLANTABLE CARDIOVERTER DEFIBRILLATOR","company": "Medtronic Inc.","city": "Minneapolis","state": "MN","country": "US","recallDate": "20240115","postedDate": "20240122","recallStatus": "Ongoing","reason": "The device may deliver inappropriate shocks due to a software defect in the detection algorithm.","rootCause": "Software defect","riskClass": "Cardiovascular","productCode": "LWS","url": "https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?id=Z-0001-2024"}
Use Cases
1. Hospital Risk Management
A biomedical engineering department runs weekly recalls for defibrillator to check whether any devices in their inventory are subject to active FDA recalls — exporting results to their asset management system.
2. Regulatory Intelligence
A MedTech consultancy monitors all recalls initiated in the last 90 days (dateFrom: 2024-01-01) for a specific therapeutic category to identify recurring failure modes ahead of a client's regulatory submission.
3. Journalist / Patient Safety Research
An investigative journalist queries recalls for breast implant since 2019 to compile a dataset of manufacturers, recall reasons and affected unit counts for a patient safety article.
Data Source
OpenFDA Device Recall API — official FDA data, updated daily.
Pricing
Pay-per-result on Apify. 500 recall records ≈ $2.50.