{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Portland",
      "state": "OR",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81935",
      "recalling_firm": "Riverpoint Medical, LLC",
      "address_1": "825 NE 25th Ave",
      "address_2": "N/A",
      "postal_code": "97232-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide Distribution in the states of IL, WA, and FL",
      "recall_number": "Z-0777-2019",
      "product_description": "RP RIVERPOINT MEDICAL 18G Brachy Grid B&K(TM) style, REF RPG-18    Product Usage:  The Riverpoint Brachytherapy Grid is used during Brachytherapy procedures to assist with the precise insertion of the needle or other probes. The Riverpoint Brachytherapy Grid is placed against the skin of the patient to help the user place the needles in a grid pattern. The letters and numbers can also correspond with computerized grids to aid in placement.",
      "product_quantity": "443 devices",
      "reason_for_recall": "Product is labeled with \"CE\", but is not yet approved in the European Union.",
      "recall_initiation_date": "20180109",
      "center_classification_date": "20190128",
      "termination_date": "20190415",
      "report_date": "20190206",
      "code_info": "Lot Numbers:  18061816, 18101521"
    }
  ]
}