{
  "meta": {
    "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.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-03-18",
    "results": {
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    {
      "status": "Ongoing",
      "city": "Richmond",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90336",
      "recalling_firm": "Mckesson Medical-Surgical Inc. Corporate Office",
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      "address_2": "Deep Run Iii Ste. 4000",
      "postal_code": "23233",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US Nationwide",
      "recall_number": "Z-1627-2022",
      "product_description": "FISHER SCIENTIFIC\tFisherbrand SWAB TRANS STUARTS DBL 50BX\t\t \t\t Catalog #1490721",
      "product_quantity": "25 Boxes",
      "reason_for_recall": "XXX",
      "recall_initiation_date": "20220525",
      "center_classification_date": "20220825",
      "report_date": "20220831",
      "code_info": "Unknown",
      "more_code_info": ""
    }
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}