{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Best",
      "state": "N/A",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89437",
      "recalling_firm": "PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.",
      "address_1": "Veenpluis 4-6",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to  AZ  CA  FL  GA  HI  IL  KS  KY  MA  MD  ME  MI  MN  MS  NC  NE  NJ  NV  NY  OH  PA  TN  TX  VA  WA  WV. Worldwide foreign distribution.",
      "recall_number": "Z-0647-2022",
      "product_description": "Zenition 50, Model #718096",
      "product_quantity": "16 US; 76 ROW",
      "reason_for_recall": "Firm discovered that the wireless foot switch can suddenly stop responding due to a firmware issue. If the wireless foot switch fails, there could be a delay or interruption of procedure if the hand switch is not used or if the wired foot switch is not connected to the system.",
      "recall_initiation_date": "20211202",
      "center_classification_date": "20220217",
      "report_date": "20220223",
      "code_info": "Wireless Foot switch 3P : 459801238191   Wireless Foot switch 3P: 459801238231"
    }
  ]
}