{
  "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": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "51 Valley Stream Pkwy",
      "reason_for_recall": "It was determined that under rare environmental conditions (i.e., extremely dry air in combination with a highly isolated floor) electrostatic discharges (ESD) >8 kV may trigger an unintended movement of the AXIOM Luminos dRFsystem which may lead to an emergency situation and pose danger to the patients, operating personnel or to the unit.",
      "address_2": "",
      "product_quantity": "37",
      "code_info": "Model number: 10094200, serial numbers:4332  4291  4323  4430  3061  4331  4238  4297  4201  4024  3098  4252  4372  4354  4077  3050  3108  4327  4342  4251  3053  3114  4156  3145  3096  4043  3181  4208  3090  4143  4051  4199  4401  4405  4151  4373  4276",
      "center_classification_date": "20140604",
      "distribution_pattern": "Class II Recall - US Distribution including the states of  IL,VA, TN, PA, TX, MN, GA, MI, IN, OH, FL, CA, OR, NY, ME, MO, OK, CO and NJ.",
      "state": "PA",
      "product_description": "AXIOM Luminos dRFsystem     The Axiom Luminos dRF is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a digital flat detector, it can perform a range of applications including general R/F, angiography and pediatric examinations. The Axiom Luminos dRF is a device intended to visualize anatomical structures by converting a pattern of X-ray into a visible image.",
      "report_date": "20140611",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1711-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68110",
      "termination_date": "20141215",
      "more_code_info": "",
      "recall_initiation_date": "20140411",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}