{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bethlehem",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65289",
      "recalling_firm": "Invatec Llc",
      "address_1": "3101 Emrick Blvd",
      "address_2": "N/A",
      "postal_code": "18020-8037",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-1517-2013",
      "product_description": "lnvatec SpA brand Diver C.E., Model/Catalog Numbers: DVR010014145,  DVR011014145,     Product is manufactured by lnvatec SpA, Roncadelle, Italy, and distributed by Invatec, Inc., Bethlehem, PA and by Medtronic Endovascular Therapies, Santa Rosa, CA  The Diver C.E. product is an aspiration catheter indicated for the removal of fresh, soft emboli and thrombi from vessels in the arterial system.",
      "product_quantity": "177 units",
      "reason_for_recall": "Devices labeled for an intended use was not included in the existing 510(k) or PMA, in that, the Indications for use was modified.",
      "recall_initiation_date": "20090304",
      "center_classification_date": "20130606",
      "termination_date": "20130610",
      "report_date": "20130612",
      "code_info": "Serial Numbers/Batches: OPI05931901, OPI05684401, OPI05684501, OPI05684601, OPI05684701, OPI05684801"
    }
  ]
}