{
  "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": "Greenville",
      "state": "SC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64529",
      "recalling_firm": "AGFA Corp.",
      "address_1": "10 S Academy St",
      "address_2": "N/A",
      "postal_code": "29601-2632",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "USA Nationwide Distribution including the states of:  AL, CA, FL, IN, MN, NE, NV, OH, SC and UT.",
      "recall_number": "Z-0970-2013",
      "product_description": "CR MD1.0 General Set, x-ray imager image plate.  CR 10-X Image Plate 35CM X 43CM.  An image plate, contained in an X-Ray cassette, used to capture images from X-Ray exposures. The cassette with the image plate, once exposed, is inserted in the Agfa Digitizer CR 10-X where the image plate is taken out of the cassette and then scanned so that the scanned image can be displayed for viewing.",
      "product_quantity": "17",
      "reason_for_recall": "The cassettes were shipped with the wrong IP (image plate) size bar code.",
      "recall_initiation_date": "20130207",
      "center_classification_date": "20130318",
      "termination_date": "20130606",
      "report_date": "20130327",
      "code_info": "Batch No. A2KQMW"
    }
  ]
}