{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96593",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2289",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US",
      "recall_number": "Z-1580-2025",
      "product_description": "Zenition 50. Product Code 718096.  The devices are used for radiological guidance and visualization during diagnostic, interventional and  surgical procedures on all patients, except neonates (birth to one month), within the limits of the devices.",
      "product_quantity": "N/A",
      "reason_for_recall": "A wireless foot switch pedal may get stuck in the active position when the user releases the pedal,  resulting in the emission of unintended radiation.",
      "recall_initiation_date": "20250225",
      "center_classification_date": "20250421",
      "report_date": "20250430",
      "code_info": "Product UDI: (01)00884838091535(21).  459801442981, Wireless foot switch set 3P (WFSS 3P)  459801238231, Wireless foot switch 3P, 459801257861, WFS Base Station 459800627394, Wireless foot switch set 3P 459800415535, Wireless foot switch 3P, 459800415542, WFS Base Station"
    }
  ]
}