{
  "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,
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  "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-2864-2018",
      "product_description": "DigitalDiagnost Upgrades (Stitching Patient Support) 712083",
      "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:   437736/SN09000282  491574/SN12000099  488712  415314/SN0902058  445533/SN10000006  414930/SN08000055  SN13000238  SN13000214  504759/SN12000356  487719/SN11000538  504766/SN12000207  SN14000264  SN14000264  469223/SN10000643  493888/SN12000004  316236  306773  306776  334582  325938  SN08000301  396570/SN0802320  SN08000216",
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}