{
  "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": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64460",
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "address_1": "9115 Hague Rd",
      "address_2": "N/A",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution.",
      "recall_number": "Z-1114-2013",
      "product_description": "CoaguChek XS Pro meters (catalog number 05530199160)bar code scanner.    Used with the CoagCHEK XS Pro Meters to quantitatively determines prothrombin time (\"PT\").",
      "product_quantity": "4467 both devices",
      "reason_for_recall": "Roche investigation into complaints found Accu-Chek Inform II and CoaguChek XS Pro System barcode reading meters had the potential of intermittent erroneous decoding of patient identification if barcodes being read fail to meet size and/or quality standards.  Errors have been confirmed with the EAN 13 barcodes which should not be used for patient or operator identification.",
      "recall_initiation_date": "20130306",
      "center_classification_date": "20130415",
      "termination_date": "20180110",
      "report_date": "20130424",
      "code_info": "catalog number 05530199160"
    }
  ]
}