{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Rochester",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "68647",
      "recalling_firm": "Carestream Health Inc.",
      "address_1": "150 Verona St",
      "address_2": "N/A",
      "postal_code": "14608-1733",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution.",
      "recall_number": "Z-2142-2014",
      "product_description": "INSIGHT Dental Film, Catalog Number/REF 811 0785, KODAK and Carestream DENTAL labels --- Carestream Health Inc.",
      "product_quantity": "1633 boxes",
      "reason_for_recall": "The Indicator Dot on the film packet's outer printed paper labeling was incorrectly positioned relative to the location of the raised dot on the dental intraoral film.  This may cause confusion for the dental practitioner.  If the processed film is placed on the view box by referencing the film's raised dot, the image orientation will be rotated 180 degrees.",
      "recall_initiation_date": "20140702",
      "center_classification_date": "20140801",
      "termination_date": "20160525",
      "report_date": "20140813",
      "code_info": "Lot Numbers: 53901201, 53801303, 53801303-1, 54601201, 54601201-1"
    }
  ]
}