{
  "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": "Williamston",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "70081",
      "recalling_firm": "Centurion Medical Products Corporation",
      "address_1": "100 Centurion Way",
      "address_2": "N/A",
      "postal_code": "48895-9086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution including MA, IN, NY, GA, AL, PA, and RI.",
      "recall_number": "Z-0945-2015",
      "product_description": "Pacemaker Tray (Cardiovascular Surgical Instruments convenience kit)",
      "product_quantity": "8 kits",
      "reason_for_recall": "According to the recall notice received from Hospira, the recall was initiated due to a confirmed customer report of particulate in a single unit. Hospira identified the particulate as human hair, embedded in and attached to a pinched area of the stopper.",
      "recall_initiation_date": "20141023",
      "center_classification_date": "20150108",
      "termination_date": "20150608",
      "report_date": "20150114",
      "code_info": "CMP Kit code: OR1955  Lot numbers: 2014061850  Expiration date: 2016-03",
      "more_code_info": ""
    }
  ]
}