{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Hertford",
      "state": "",
      "country": "United Kingdom",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95786",
      "recalling_firm": "Spacelabs Healthcare, Ltd.",
      "address_1": "Unit B",
      "address_2": "Foxholes Centre; John Tate Road",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: AR, CA, CO, DE, FL, FA, LA, MA, MI, MN, MT, NC, NE, NU OH, OR, PA, Puerto Rico, TN, TX, UT, VA, WA, and WI.  O.U.S.: Argentina Denmark Kuwait Serbia Australia Dominican Republic Lebanon Singapore Austria Ecuador Lithuania Spain Belgium El Salvador Martinique Sweden Benin France Mexico Switzerland Bolivia Germany Netherlands Taiwan Brazil Greece Oman Trinidad and Tobago Brunei Darussalam Guatemala Panama Turkey Canada Honduras Peru United Arab Emirates Chile Hong Kong Poland United Kingdom China Iceland Portugal Columbia India Venezuela Congo Ireland Qatar Viet Nam Costa Rica Israel Republic of Macedonia Croatia Italy Roumanie Czech Republic Korea, Republic of Saudi Arabia",
      "recall_number": "Z-0685-2025",
      "product_description": "Eclipse Mini REF 98900    The Eclipse MINI Model 98900 is a portable non-invasive continuous ambulatory ECG patch recorder intended to record the patient s electrocardiogram.",
      "product_quantity": "1,779 devices",
      "reason_for_recall": "Due to a manufacturing error the incorrect device serial number was potentially programmed into the holter recorder.  The physical serial number label on the device might not match the serial number programmed into the device.",
      "recall_initiation_date": "20241125",
      "center_classification_date": "20241217",
      "report_date": "20241225",
      "code_info": "Model Number: 98900 UDI-DI code: 10841522128769 Serial Numbers:  All serial numbers manufactured between May 2021 to November 2024.  Serial Numbers pending.",
      "more_code_info": ""
    }
  ]
}