{
  "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": "Ongoing",
      "city": "Billerica",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91376",
      "recalling_firm": "Conformis, Inc.",
      "address_1": "600 Technology Park Dr Ste 3",
      "address_2": "N/A",
      "postal_code": "01821-4154",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AL, AZ, CO, FL, GA, KS, KY, LA, MA, MD, MS, NE, NH, NV, NY, OH, TN, WI, WY.",
      "recall_number": "Z-1133-2023",
      "product_description": "iTotal Identity Impactor Handle, Model No. 1080-212/ED-07827 REV AE",
      "product_quantity": "70",
      "reason_for_recall": "Loctite thread locker (epoxy) may not have been applied to the screw that is part of the handle. In the absence of epoxy, the screw may loosen and fall into the patient during a procedure.",
      "recall_initiation_date": "20221114",
      "center_classification_date": "20230213",
      "report_date": "20230222",
      "code_info": "UDI-DI 00810933030582  Lot D221301"
    }
  ]
}