{
  "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": [
    {
      "country": "United States",
      "city": "Malvern",
      "address_1": "40 Liberty Blvd",
      "reason_for_recall": "Potential issue leading to data loss and patient data mix-up",
      "address_2": "Mail Code: 65-1A",
      "product_quantity": "37",
      "code_info": "Model Number of device   10592457  with serial numbers: Serial  100544  100499  100600  100571  100263  200308  200309  200310  200311  200312  200313  200314  200315  200316  200317  200318  200319  200320  200321  200322  200323  200324  100146  200277  100177  100138  100174  100491  100492  100596  100198  100181  200251  200252  100301  100302  100539",
      "center_classification_date": "20150902",
      "distribution_pattern": "US Nationwide Distribution - in the states of CA, OR, FL, MO, NY, WA, MD, MA, NY, WI, KS, MN and PA.",
      "state": "PA",
      "product_description": "Syngo.plaza; picture archiving and communications system    Product Usage:  Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning. Syngo.plaza also supports storage and archiving of DICOM Structured reports. In a comprehensive imaging syngo.plaza integrates Hospital/Radiology Information Systems (HIS/RIS) to enable customer specific workflows. Syngo.plaza optionally uses a variety of advanced postprocessing applications.",
      "report_date": "20150909",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-2719-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71978",
      "termination_date": "20170106",
      "recall_initiation_date": "20150706",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}