{
  "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": "2026-08-20",
    "results": {
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      "limit": 1,
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  "results": [
    {
      "cfres_id": "114053",
      "product_res_number": "Z-0515-2013",
      "event_date_initiated": "2012-10-10",
      "event_date_posted": "2012-12-12",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-11-06",
      "res_event_number": "63496",
      "product_code": "FSY",
      "k_numbers": [
        "K063333"
      ],
      "product_description": "MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system\n\nCeiling mounted surgical light",
      "code_info": "Part numbers 7721165, 4787714, 7559375, 10281150, 10281151, 10281152 and 10281183",
      "firm_fei_number": "2240869",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "city": "Malvern",
      "state": "PA",
      "postal_code": "19355",
      "additional_info_contact": "Customer Support\n610-219-6300",
      "reason_for_recall": "A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.",
      "root_cause_description": "Equipment maintenance",
      "action": "Siemens sent a Customer Safety Advisory Notice on October 3, 2012, to all affected customers.  The Notice identified the product, the problem, and the action to be taken by the customer.   Customers were reminded that they should contact the service department in the event of damage or other irregularity.  Customers were instructed to forward the information contained in the notice to their employees responsible for the operation of the affected product.  Customers were also asked to forward the safety information to other organization affected by the product and to any users of the product.\nFor questions regarding this recall call 610-219-4834.",
      "product_quantity": "1315",
      "distribution_pattern": "Nationwide Distribution",
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        "device_name": "Light, Surgical, Ceiling Mounted",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4580",
        "device_class": "2"
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}