{
  "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": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "75499",
      "recalling_firm": "OMNI LIFE SCIENCE",
      "address_1": "480 Paramount Dr",
      "address_2": "N/A",
      "postal_code": "02767-1085",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution: US distribution to OK, MD, TX and country of:  Australia.",
      "recall_number": "Z-0610-2017",
      "product_description": "OMNIBotics Tracker Kit -Model: RM-10000     The TOTAL KNEE SURGETICS Navigation System with iBlock (Now OMNIBotics) is intended for use during stereotaxic surgery to aid the surgeon in locating anatomical structures and aligning the endoprostheses with the anatomical structures. It is specifically indicated for: Total Knee Arthroplasty",
      "product_quantity": "15 units",
      "reason_for_recall": "Incorrect lot number on outer kit",
      "recall_initiation_date": "20161014",
      "center_classification_date": "20161117",
      "termination_date": "20170201",
      "report_date": "20161123",
      "code_info": "Lot  number: 19-09-021"
    }
  ]
}