{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waterbury",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88345",
      "recalling_firm": "Northeast Scientific Inc.",
      "address_1": "2142 Thomaston Ave",
      "address_2": "N/A",
      "postal_code": "06704-1013",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of CA, CT, FL, GA, IL, MA, NC, NJ, NY, TX.",
      "recall_number": "Z-2334-2021",
      "product_description": "NES Reprocessed Visions PV .035 IVUS Catheter, Sterile.    For use in the evaluation of vascular morphology in blood vessels of the peripheral vasculature by providing a crosssectional image of such vessels.     NES Ref. No. R-88901",
      "product_quantity": "690 devices",
      "reason_for_recall": "510k indicated one (1) reprocessing cycle, product not cleared for additional reprocessing cycles.",
      "recall_initiation_date": "20210426",
      "center_classification_date": "20210823",
      "termination_date": "20220309",
      "report_date": "20210901",
      "code_info": "Lots L0017886 through L0020553"
    }
  ]
}