{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91294",
      "recalling_firm": "NuVasive Inc",
      "address_1": "7475 Lusk Blvd",
      "address_2": "",
      "postal_code": "92121-5707",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide distribution in the states of CA, FL, NC, OH, and TX.",
      "recall_number": "Z-1052-2023",
      "product_description": "NuVasive MD Pulse III Multimodality System REF 1881500    Pulse Software version 369-BL.US and 369-BLN.US",
      "product_quantity": "7",
      "reason_for_recall": "Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and upper and lower extremity procedures.",
      "recall_initiation_date": "20220719",
      "center_classification_date": "20230203",
      "report_date": "20230215",
      "code_info": "Part Number: 1881500 UDI Code: 0887517PLS137YJ Serial Numbers: PM00017 SM90018 SM90013 SM90021 PM00007 SM90032 SM90030",
      "more_code_info": ""
    }
  ]
}