{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69613",
      "recalling_firm": "Zimmer, Inc.",
      "address_1": "1800 W Center St",
      "address_2": "N/A",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US nationwide distribution.",
      "recall_number": "Z-0574-2015",
      "product_description": "Zimmer Title 2 Bone Screw Remover Instrument, Part Number ET1093-01 Rx Only, Non-Sterile.    The Screw Remover is a component of the Endius TITLE 2 Polyaxial Spinal System, used for posterior lumbar fusion procedures.",
      "product_quantity": "14 devices",
      "reason_for_recall": "Possibility of the weld to the quick-connect  breaking when force is applied to the handle for pedicle screw removal.  A broken weld could lead to the use of an alternate method of screw removal, which could delay surgery up to 30 minutes.",
      "recall_initiation_date": "20130826",
      "center_classification_date": "20141209",
      "termination_date": "20150224",
      "report_date": "20141217",
      "code_info": "Lot:  L75066"
    }
  ]
}