{
  "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-2857-2018",
      "product_description": "DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052",
      "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:   422102/SN0902020  435210/SN0902204  460471/SN1002019  433651/SN0902114  427610/SN0902108  470160/SN1102003  447013/SN1002008  445778/SN1002006  420208/SN0902019",
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}