{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Portland",
      "address_1": "825 NE 25th Ave",
      "reason_for_recall": "The integrity of the sterile grid packaging is potentially compromised.",
      "address_2": "",
      "product_quantity": "3,234 devices",
      "code_info": "Lot numbers 16032422, 16051814, 16051815, 16052425, 17042430, 17050936, 17052532, 17061214, 17121823, 17122820, 18040922, 18061816, 18101521, and 18120705; UDI number 00812444028638.",
      "center_classification_date": "20200110",
      "distribution_pattern": "Distribution was made to IL, FL, TX, and WA.  There was no foreign/military/government distribution.",
      "state": "OR",
      "product_description": "Riverpoint Medical 18G Brachy Grid, B&K style, REF RPG-18, Sterile, Rx.  The firm name on the label is Riverpoint Medical, LLC, Portland, OR.",
      "report_date": "20200122",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Riverpoint Medical, LLC",
      "recall_number": "Z-0795-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84528",
      "termination_date": "20210428",
      "more_code_info": "",
      "recall_initiation_date": "20190208",
      "postal_code": "97232-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}