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Find FDA aspirin recall records and resolve one recall number.
1Request
number

limit

string

Plain openFDA search expression, e.g. product_description:aspirin or report_date:[20250101 TO 20251231]. Use spaces around AND, OR and TO; do not URL-encode the expression or use + as a space. Literal plus signs are preserved. Mutually exclusive with record_id. Omit both to browse source default order.

string

Source identifier returned by this dataset. Exact quoted lookup; mutually exclusive with query.

5 credits
Codefollows the fields above
const result = await firecrawl.scrape({
  alexandria: {
    provider: "fda-gov",
    capability: "records/device_clearances",
    options: {
      limit: 1,
    },
  },
});
2Response example

This is a sample shape. Press Run to see live data from FDA.

{
  "dataset": "device_clearances",
  "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
  "last_updated": "2026-09-07",
  "next_skip": 1,
  "observed_at_ms": 1789509514341,
  "pagination_truncated": false,
  "records": [
    {
      "data": {
        "address_1": "9705 International Ct. N.",
        "address_2": "",
        "advisory_committee": "",
        "advisory_committee_description": "Unknown",
        "applicant": "Bioderm, Inc.",
        "city": "St. Petersburg",
        "clearance_type": "Traditional",
        "contact": "MARIE B TEIXEIRA",
        "country_code": "US",
        "date_received": "1998-08-21",
        "decision_code": "SESE",
        "decision_date": "1998-10-13",
        "decision_description": "Substantially Equivalent",
        "device_name": "BTF THIN FILM WOUND DRESSING",
        "expedited_review_flag": "",
        "k_number": "K982939",
        "openfda": {
          "device_class": "U",
          "device_name": "Dressing, Wound And Burn, Occlusive",
          "fei_number": [
            "3014562978",
            "3005012805",
            "3041276591",
            "1000305720",
            "1000117748",
            "3031168520",
            "3010419931",
            "3012421607",
            "3002807111",
            "3004365956",
            "3005747797",
            "3010034780",
            "3030733800",
            "3010041511",
            "3002806830",
            "1219313",
            "3003636207",
            "1526534",
            "3012494290",
            "3012502601",
            "3013557562",
            "3001451571"
          ],
          "medical_specialty_description": "Unknown",
          "registration_number": [
            "3014562978",
            "3005012805",
            "3041276591",
            "3031168520",
            "1320894",
            "3010419931",
            "3012421607",
            "9680091",
            "3004365956",
            "3010034780",
            "3011137372",
            "3030733800",
            "3010041511",
            "3005941719",
            "1219313",
            "3003636207",
            "1526534",
            "3012494290",
            "1223925",
            "1644312",
            "3012502601",
            "3013557562"
          ],
          "regulation_number": ""
        },
        "postal_code": "33716",
        "product_code": "MGP",
        "review_advisory_committee": "SU",
        "state": "FL",
        "statement_or_summary": "Summary",
        "third_party_flag": "N",
        "zip_code": "33716"
      },
      "record_id": "K982939",
      "source_url": "https://api.fda.gov/device/510k.json?search=k_number%3A%22K982939%22&skip=0&limit=1"
    }
  ],
  "skip": 0,
  "source_url": "https://api.fda.gov/device/510k.json?skip=0&limit=1",
  "total_matching": 176070
}

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