{
  "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": "Ventura",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66208",
      "recalling_firm": "Implantech Associates Inc",
      "address_1": "6025 Nicolle St Ste A",
      "address_2": "N/A",
      "postal_code": "93003-7602",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (nationwide) including states of NY, KY, and CO, and the country of Israel.",
      "recall_number": "Z-2211-2013",
      "product_description": "Device Name: Terino Square Chin-Style II-Medium; Catalog Number: TSCII-M.    To augment or reconstruct underdeveloped or traumatized mandibular region.",
      "product_quantity": "8",
      "reason_for_recall": "Implantech initiated a voluntary recall of certain lots of Terino Square Chin-Style II-Medicum (Lot # 848488 and 850156), after determining that the devices from the lot numbers do not conform to the dimensional requirements for the TSCII-M.",
      "recall_initiation_date": "20130830",
      "center_classification_date": "20130917",
      "termination_date": "20140206",
      "report_date": "20130925",
      "code_info": "Catalog Number: TSCII-M  Lot Numbers: 848488 and 850156",
      "more_code_info": ""
    }
  ]
}