{
  "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": "Broomfield",
      "state": "CO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69615",
      "recalling_firm": "Biomet Spine LLC.",
      "address_1": "310 Interlocken Pkwy Ste 120",
      "address_2": "N/A",
      "postal_code": "80021-3464",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Nationwide Distribution in the states of California, Indiana, Louisiana, and Texas,",
      "recall_number": "Z-0220-2015",
      "product_description": "LANX, REF, PCR8XXX-XXX, LOT, RXONLY.  Packaged within aluminum sterilization case.    Product Usage:  The Durango implant is intended for spinal fusion procedures to be used with autogenous bone graft in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous spinal levels from L2S1.",
      "product_quantity": "120",
      "reason_for_recall": "Biomet Spine, LLC. announces voluntary recall of Durango Anchored ALIF Plate due to the set screw component potentially becoming dislodged from the plate assembly.",
      "recall_initiation_date": "20110309",
      "center_classification_date": "20141114",
      "termination_date": "20150107",
      "report_date": "20141126",
      "code_info": "Lot numbers L532655, L532690, Product code 8503\u0010XXXX"
    }
  ]
}