{
  "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": {
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  "results": [
    {
      "status": "Terminated",
      "city": "Coconut Creek",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92005",
      "recalling_firm": "New Wave Endo-Surgical, Corp.",
      "address_1": "6601 Lyons Rd Ste D8",
      "address_2": "N/A",
      "postal_code": "33073-3630",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide distribution in the states of FL, MA, and GA.",
      "recall_number": "Z-1570-2023",
      "product_description": "M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall",
      "product_quantity": "295 units",
      "reason_for_recall": "The plastic housing on the device may fracture",
      "recall_initiation_date": "20200708",
      "center_classification_date": "20230509",
      "termination_date": "20240702",
      "report_date": "20230517",
      "code_info": "UDI/DI:  00850009417022, Lot code C2020"
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}