{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Burnsville",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94279",
      "recalling_firm": "Advanced Research Medical, LLC",
      "address_1": "1515 Highway 13 E",
      "address_2": "",
      "postal_code": "55337-2917",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of Minnesota.",
      "recall_number": "Z-1698-2024",
      "product_description": "ADVANCED RESEARCH MEDICAL Lumbar Interbody Fusion System (OLLIF), Flexible Curette Loop Blade, Part # 01-06-4; treatment of degenerative disc disease",
      "product_quantity": "1150 units",
      "reason_for_recall": "Potential shearing of the disposable blade may occur and be contained within the of Flexible Curette Shaft Assembly during surgery.",
      "recall_initiation_date": "20230314",
      "center_classification_date": "20240429",
      "report_date": "20240508",
      "code_info": "UDI/DI 00850014575311, Lot Numbers:  87458, BB059AA, BB140AA, BB140AB, BB307AA, BB350AA, BC061AA, BC130AA, BC130AA-2, BC274AA, BD083AA, BD083AB, BD083AC",
      "more_code_info": ""
    }
  ]
}