{
  "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": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68781",
      "recalling_firm": "Innovasis, Inc",
      "address_1": "614 E 3900 S",
      "address_2": "N/A",
      "postal_code": "84107-1902",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Distribution US nationwide, including TX, CA, KS, MN, and OK. Foreign distribution to Japan.",
      "recall_number": "Z-2067-2014",
      "product_description": "Excella II Standard Pedicle Screw, Catalog No. E2S47525 and E2S47535, 4.75 mm x 25 mm. For spinal fixation.   Packaged in heat-sealed plastic bag. Also provided in reusable steam sterilization tray as implant set.",
      "product_quantity": "32",
      "reason_for_recall": "Innovasis is recalling the Excella II Standard Pedicle Screw due to mislabeling of the size and catalog number.",
      "recall_initiation_date": "20140707",
      "center_classification_date": "20140716",
      "termination_date": "20140811",
      "report_date": "20140723",
      "code_info": "E2S47525 Lot 1301 and E2S47535 Lot 1301"
    }
  ]
}