{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Terminated",
      "city": "Plano",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87595",
      "recalling_firm": "Krishe Inc",
      "address_1": "8105 Razor Blvd Ste 213",
      "address_2": "N/A",
      "postal_code": "75024",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: LA, TX, FL, GA",
      "recall_number": "Z-1421-2021",
      "product_description": "Dasky Disposable Sampling Tube, REF VSM02, Contents: Transport Media - 50, Nasal swab - 50, Package Insert - 1, IVD, CE",
      "product_quantity": "441,500 units",
      "reason_for_recall": "Verification and validation of the virus transport medium tubes was not provided to FDA prior to sale and marketing",
      "recall_initiation_date": "20210311",
      "center_classification_date": "20210413",
      "termination_date": "20221116",
      "report_date": "20210421",
      "code_info": "All Lots"
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}