{
  "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": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "73292",
      "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": "US Distribution including Puerto Rico and to the states of :TX, OH, TN, AZ, WA, MI and GA",
      "recall_number": "Z-1233-2016",
      "product_description": "cobas p 512 pre-analytical system    Pre-analytical sample handling that includes de-capping, aliquoting and sorting of samples for analysis.",
      "product_quantity": "35 Units",
      "reason_for_recall": "Due to a false triggering or detection of the lifting gripper READY signal, sample tubes are not correctly placed back in the Rack Tube Transport (RTT) after the decapping process. Therefore, open sample tubes can be dropped in the cobas p 512, spilling the sample material.",
      "recall_initiation_date": "20160223",
      "center_classification_date": "20160323",
      "termination_date": "20180111",
      "report_date": "20160330",
      "code_info": "Part numbers:05083435001 and 06268854001"
    }
  ]
}