{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "66143",
      "recalling_firm": "Camlog Usa",
      "address_1": "5315 W 74th St Ste 200",
      "address_2": "N/A",
      "postal_code": "46268-5136",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "USA Distribution in the states of  NH, MD, CO, and IL.",
      "recall_number": "Z-2203-2013",
      "product_description": "C2244.3808, CONELOG Titanium Base CC ¿3.8GH0.8 inkl HS    Product Usage:  Endosseous dental implant abutment CONELOG Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CONELOG implants to support prostheses in the maxillary and/or mandibular arch.",
      "product_quantity": "2 in USA",
      "reason_for_recall": "Product not cleared for sale/use in the United States.",
      "recall_initiation_date": "20130828",
      "center_classification_date": "20130916",
      "termination_date": "20140129",
      "report_date": "20130925",
      "code_info": "43746",
      "more_code_info": ""
    }
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}