{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63496",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "address_2": "N/A",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0515-2013",
      "product_description": "MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system    Ceiling mounted surgical light",
      "product_quantity": "1315",
      "reason_for_recall": "A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.",
      "recall_initiation_date": "20121010",
      "center_classification_date": "20121212",
      "termination_date": "20141106",
      "report_date": "20121219",
      "code_info": "Part numbers 7721165, 4787714, 7559375, 10281150, 10281151, 10281152 and 10281183"
    }
  ]
}