{
  "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": "Ongoing",
      "city": "North Haven",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80804",
      "recalling_firm": "Covidien LLC",
      "address_1": "60 Middletown Ave",
      "address_2": "N/A",
      "postal_code": "06473-3908",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign: Australia, New Zealand",
      "recall_number": "Z-2958-2018",
      "product_description": "Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems.  Product Number/CFN: 186-0208  UDI-Device Identifier (GTIN/UPN): 10884521130319",
      "product_quantity": "BIS 46,961; Spare Batteries: 6,937",
      "reason_for_recall": "Revised replacement instructions for the Li-ion battery packs used in BIS Vista and BIS View Monitoring Systems",
      "recall_initiation_date": "20180726",
      "center_classification_date": "20180830",
      "report_date": "20180905",
      "code_info": "Batteries with date code 3114 or older (Week 31 of 2014)"
    }
  ]
}