{
  "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": "Hamburg",
      "state": "",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80577",
      "recalling_firm": "Philips Medical Systems Gmbh, DMC",
      "address_1": "Development And Manufacturing Ctr.",
      "address_2": "Rontgenstr. 24",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide; International to 66 countries",
      "recall_number": "Z-2845-2018",
      "product_description": "DigitalDiagnost Release 3.1 (Stitching Patient Support) 712026",
      "product_quantity": "",
      "reason_for_recall": "The hook does not securely hold the footplate in the vertical position.  Therefore, the footplate can fall or swing down and injury operator or patient.",
      "recall_initiation_date": "20180627",
      "center_classification_date": "20180817",
      "termination_date": "20240430",
      "report_date": "20180829",
      "code_info": "Serial Numbers:   SN13000495  SN14000058  SN13000463  SN14000051  SN14000214  SN14000047  SN14000077  SN13000484  SN14000082  SN14000163  SN14000133  SN14000134  SN14000134  SN14000023  SN14000041",
      "more_code_info": ""
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}