{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Hartland",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88379",
      "recalling_firm": "Merge Healthcare, Inc.",
      "address_1": "900 Walnut Ridge Dr",
      "address_2": "N/A",
      "postal_code": "53029-8347",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US distribution",
      "recall_number": "Z-2387-2021",
      "product_description": "Merge Hemo, Software packages 10.2, 10.3, and 10.4",
      "product_quantity": "326 units",
      "reason_for_recall": "The firm identified a safety issue affecting the software associated with Merge Hemo versions 9.x and 10.x, used in combination with an HL7 lab interface.",
      "recall_initiation_date": "20210723",
      "center_classification_date": "20210828",
      "termination_date": "20230829",
      "report_date": "20210908",
      "code_info": "Version 10.2, UDI (01)00842000100430(10)10.2(11)190612  Version 10.3, UDI (01)00842000100874(10)10.3(11)200330  Version 10.4, UDI (01)00842000100966(10)10.4(11)210428"
    }
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}