{
  "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": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Rd",
      "reason_for_recall": "The thickness of the connector to the trunk cable on affected limb lead sets may be greater than specified. which may prevent or impede the performance of I 2-Lead ECG measurements.",
      "address_2": "",
      "product_quantity": "280 boxes ( 5600 leadsets)",
      "code_info": "Lot codes: 03/18, 05/18 and 06/18",
      "center_classification_date": "20190909",
      "distribution_pattern": "Worldwide Distribution - US Nationwide   State  KY  AZ  CA  UT  OH  NY  SC  CO  FL  IN  TX  ND  KS  GA    Canada  Germany",
      "state": "MA",
      "product_description": "Philips 5-Lead Set, Disposable, Bedside, AAMI  Model # 989803173131    Product Usage:  Philips Single-Patient-Use ECG lead sets for bedside monitoring are available in 5-lead configuration",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips North  America, LLC",
      "recall_number": "Z-2495-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83560",
      "termination_date": "20200603",
      "more_code_info": "",
      "recall_initiation_date": "20190719",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}