{
  "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": [
    {
      "country": "United States",
      "city": "Mequon",
      "address_1": "6140 W Executive Dr",
      "reason_for_recall": "Titan Spine is recalling specific Endoskeleton TCS Integrated Locking Bone Screw Assembly due to the locking bone screw collars not 'locking'.",
      "address_2": "Suite A",
      "product_quantity": "137 units",
      "code_info": "Lot numbers:  V03, V05, V06",
      "center_classification_date": "20150803",
      "distribution_pattern": "Distributed in the states of CA, TX, OK, MA, NY, IN, OR, and GA.",
      "state": "WI",
      "product_description": "Titan Spine Endoskeleton Locking Bone Screw Assembly, which is part of the Endoskeleton TCS Interbody Fusion Device, spinal implant.  Part Numbers / Product Description:  5302-3514 / 03.5 x 14mm Locking Screws;   5302-3516 / 03.5 x 16mm Locking Screws;    502-3518 / 03.5 x 18mm Locking Screws;  5302-3814 / 03.8 x 14mm Locking Screws;  5302-3816 / 03.8 x 16 mm Locking Screws;    5302-3818 / 03.8 x 18mm Locking Screws.",
      "report_date": "20150812",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "TITAN SPINE, LLC",
      "recall_number": "Z-2327-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71740",
      "termination_date": "20151020",
      "recall_initiation_date": "20150720",
      "postal_code": "53092-4499",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}