{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Indianapolis",
      "state": "IN",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82651",
      "recalling_firm": "Roche Diagnostics Corporation",
      "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 Nationwide Distribution in the states of AL, CA, FL, IA, IL, KY, MD, OR & PA",
      "recall_number": "Z-1927-2019",
      "product_description": "cobas p 501 post-analytical units, Part Number 05158494001.  For diagnostic sample storage and retrieval.",
      "product_quantity": "4 units",
      "reason_for_recall": "There is a potential for the tray input flap on the post analytical units to become loose, potentially detaching from the instrument.",
      "recall_initiation_date": "20190404",
      "center_classification_date": "20190702",
      "termination_date": "20200512",
      "report_date": "20190710",
      "code_info": "Serial Numbers - 1001 through 1044"
    }
  ]
}