{
  "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": "72427",
      "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": "E-Mail",
      "distribution_pattern": "Distributed to TX only.",
      "recall_number": "Z-0297-2016",
      "product_description": "Bulk Loader Module for cobas p 512/612  Pre-analytical sample handling that includes de-capping, aliquoting and sorting of samples for analysis.   In vitro diagnostic machine component.",
      "product_quantity": "1",
      "reason_for_recall": "Possible for sample tubes in the loader to be opened and contaminate the system as well as adjacent samples during processing.",
      "recall_initiation_date": "20150922",
      "center_classification_date": "20151118",
      "termination_date": "20160203",
      "report_date": "20151125",
      "code_info": "During transport from the Bulk Loader Module (BLM), catalog number 07135645001, to the cobas p 512/p 612 pre-analytical instruments, sample tubes may inadvertently open and spill, causing  contamination of the system."
    }
  ]
}