{
  "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": "2026-04-15",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Plymouth",
      "address_1": "14405 21st Ave N Ste 130",
      "reason_for_recall": "Possible compromise of the sterile barrier integrity",
      "address_2": "",
      "product_quantity": "1200 units",
      "code_info": "UDI 10867516000101  Lot Number 182801",
      "center_classification_date": "20181005",
      "distribution_pattern": "Israel",
      "state": "MN",
      "product_description": "INSORB SUBCUTICULAR SKIN STAPLER, REF 2030",
      "report_date": "20181017",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Incisive Surgical Inc",
      "recall_number": "Z-0078-2019",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "81008",
      "termination_date": "20190318",
      "more_code_info": "",
      "recall_initiation_date": "20180829",
      "postal_code": "55447-4638",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}