{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Best",
      "state": "N/A",
      "country": "Netherlands",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82610",
      "recalling_firm": "Philips Medical Systems Nederlands",
      "address_1": "Veenpluis 4-6",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to state of: FL and Internationally to: Switzerland and Germany.",
      "recall_number": "Z-1240-2019",
      "product_description": "Ingenia Ambition S (781359), Ingenia Ambition X (781356) with Magnet Energization Device (MED),     Philips MR systems are indicated for use as a diagnostic device. The purpose of the MED is to supply power to charge the magnet. MED is abbreviation for Magnet Energize Device",
      "product_quantity": "4 units",
      "reason_for_recall": "Magnet Energization Device (MED) can have a residual voltage on output terminal, may cause electrical shocks to personnel servicing the MED, MDD or connected cabling.",
      "recall_initiation_date": "20190325",
      "center_classification_date": "20190426",
      "termination_date": "20200604",
      "report_date": "20190508",
      "code_info": "US Serial Number: 47004  OUS Serial Numbers: 47001, 47002, 48000"
    }
  ]
}