{
  "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,
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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-2848-2018",
      "product_description": "DigitalDiagnost 2.x Upgrades (Stitching Patient Support) 712081",
      "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:   428633/SN09000234  430908/SN09000165  487800/SN11000531",
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