{
  "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": {
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      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Heidelberg",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97509",
      "recalling_firm": "MedicalCommunications GmbH",
      "address_1": "Max-Jarecki-Str. 8",
      "address_2": "N/A",
      "postal_code": "N/A",
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      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution.",
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      "product_description": "Ashvins variant HEYEX 2 / HEYEX PACS. Software Version: Version 2.6.0 (Build 2088) to 2.6.8 (Build 2220).    Device Type: Software (Medical Image Management, Picture Archiving and Communication System)",
      "product_quantity": "474 units",
      "reason_for_recall": "Potential that the measured value may be smaller than the actual area.",
      "recall_initiation_date": "20250909",
      "center_classification_date": "20250930",
      "report_date": "20251008",
      "code_info": "Model Name: Ashvins variant HEYEX 2 / HEYEX PACS. UDI-DI: 4260648620046. Software Version: 2.6.0 (Build 2088) to 2.6.8 (Build 2220)."
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}