{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Mateo",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94270",
      "recalling_firm": "ROUTE 92 MEDICAL INC",
      "address_1": "155 Bovet Rd Ste 100",
      "address_2": "N/A",
      "postal_code": "94402-3151",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US: AL\tAZ\tCA\tDE\tFL\tGA\tIA\tIL\tIN\tKY\tLA\tMA\tMD\tMI\tMN\tMO\t NC ND\tNJ\tNY\tOH\tOR\tPA\tRI\tSD\tTN\tTX\tUT\tVA\tWV  OUS: New Zealand",
      "recall_number": "Z-1612-2024",
      "product_description": "Route 92 Medical, 070 Access System,  REF 1004, Rxonly , Sterile EO. Used for introduction of interventional devices into the neurovasculature.",
      "product_quantity": "117 units",
      "reason_for_recall": "Their is the potential for distal tip separation at the proximal marker band of the delivery catheters",
      "recall_initiation_date": "20240308",
      "center_classification_date": "20240424",
      "report_date": "20240501",
      "code_info": "UDI: 00853799007442/ Lot #  23061601  24010306, 23081802, 24011801, 23100601,  24020801, 23102601",
      "more_code_info": ""
    }
  ]
}