{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "Vibrations of the C-arm of the plane B may result in reduced image quality caused by the screw connection to the C-arm in the ceiling support",
      "address_2": "",
      "product_quantity": "54 units",
      "code_info": "Serial Numbers:  121336  121368  121208  121371  121374  121209  121325  121357  121378  121369  121364  121314  121351  121354  121340  121365  121324  121216  121333  121381  121352  121355  121210  121215  121379  121366  121323  121370  121384  121332  121344  121309  121305  121342  121301  121315  121372  121321  121383  121312  121359  121322  121356  121319  121211  121375  121377  121361  121339  121310  121362  121316  121212  121313",
      "center_classification_date": "20181113",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "PA",
      "product_description": "ARTIS Q biplane with Material 10848282-  - a Angiographic x-ray system    Product Usage:  Artis zee is a dedicated angiography system developed for single and biplane diagnostic imaging and interventional procedures including, but not limited to, pediatric and obese patients. Procedures that can be performed with the Artis zee includes cardiac angiography, neuro angiography, general angiography, rotational angiography, operating room angiography, multipurpose angiography and whole body radiographic/fluoroscopic procedures. Artis zee can also support the acquisition of position triggered imaging for spatial data synthesis.",
      "report_date": "20181121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-0458-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81514",
      "termination_date": "20200427",
      "more_code_info": "",
      "recall_initiation_date": "20181019",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}