{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "74799",
      "recalling_firm": "Straumann Manufacturing, Inc.",
      "address_1": "60 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1008",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-2535-2016",
      "product_description": "Straumann Bone Level Implant, ¿ 4.1mm RC, SLA¿ 12mm, TiZr, NTP  Article Number: 021.4512",
      "product_quantity": "33 pieces",
      "reason_for_recall": "Misalignment with the Loxim transfer piece markings, the positioning of the implant will be incorrect for optimal restoration",
      "recall_initiation_date": "20160714",
      "center_classification_date": "20160812",
      "termination_date": "20201120",
      "report_date": "20160824",
      "code_info": "Lot Number:  LT123"
    }
  ]
}