{
  "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-2862-2018",
      "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:   SN14000256  SN14000250  SN15000024  SN14000170  SN14000052  SN14000224  SN15000039  SN14000144  SN14000253  SN14000239  SN14000186  SN14000075  SN14000193  SN14000254  SN15000001  SN14000089  SN14000223  SN14000267  SN14000238  SN14000164  SN14000165  SN14000200  SN14000005  SN14000040  SN15000015  SN15000029  SN14000120",
      "more_code_info": ""
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}