{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Nottingham",
      "state": "N/A",
      "country": "United Kingdom",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98292",
      "recalling_firm": "SUREPULSE MEDICAL LTD",
      "address_1": "Medicity D6 Thane Road",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CT, TX and the countries of United Kingdom of Great Britain and Northern Ireland, Netherlands, United Arab Emirates.",
      "recall_number": "Z-1360-2026",
      "product_description": "Surepulse VS Cap Extra Large  REF: SP-163-A1  component of VS Newborn Heart Rate Monitor",
      "product_quantity": "N/A",
      "reason_for_recall": "Retroactively reported; Labeling  contains incorrect sizing guide for Cap, a component of the heart rate monitor.",
      "recall_initiation_date": "20230120",
      "center_classification_date": "20260212",
      "report_date": "20260218",
      "code_info": "DI Number: 05060550650044/Lot:  13816/00001 13817/00001 13818/00001 13819/00001 13820/00001 13821/00001 13822/00001 13823/00001 13824/00001 13825/00001 13826/00001 13827/00001 13828/00001 13829/00001 13830/00001 13831/00001 13832/00001 13833/00001 13834/00001 13835/00001 13836/00001 13837/00001 13838/00001 13839/00001 13840/00001"
    }
  ]
}