{
  "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": "72878",
      "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": "Letter",
      "distribution_pattern": "Distributed in US -- CA; KS; OH; & TX.",
      "recall_number": "Z-0662-2016",
      "product_description": "Excella II Rod  Cat. No.: SR 55100 5.5 x 100 mm LOT 1502  and Excella II Rod Cat. No.: SR 55110 5.5 x 110 mm LOT 1502  Packaged in heat-sealed plastic bag. Also provided in reusable steam sterilization tray as implant set.    Intended for use in the non-cervical area of the spine.",
      "product_quantity": "17 units Labeled SR55100 Lot 1502 with SR55110 rods in package",
      "reason_for_recall": "Innovasis recalled two lots of Excella II titanium rods which were packaged using each other's labels.",
      "recall_initiation_date": "20151207",
      "center_classification_date": "20160119",
      "termination_date": "20160407",
      "report_date": "20160127",
      "code_info": "Catalog No.: SR55110 Lot 1502 and SR55100 Lot 1502",
      "more_code_info": ""
    }
  ]
}