{
  "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": "Potential patient data mixup.  Improper error handling could allow for two different patients to be displayed in syngo Dynamics.  Images shown for one patient and reporting system shown for a different patient, leading to the potential for misdiagnosis.",
      "address_2": "",
      "product_quantity": "50",
      "code_info": "Model nos.10091804, 10091805, 10091806, 10091807, 10091673.  syngo Dynamics Version 9.5 using Sensis integration.",
      "center_classification_date": "20140318",
      "distribution_pattern": "Nationwide distribution to MN, AR, MA, TX, NJ, WV, GA, CA, PA, OH, MI, WI, TN, NY, KS, CT, NY, MO, IL, IN, OR, IA, and WA.",
      "state": "PA",
      "product_description": "syngo Dynamics  Picture Archiving and Communication System (PACS).  Model numbers 10091804, 10091805, 10091806, 10091807, 10091673",
      "report_date": "20140326",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "recall_number": "Z-1216-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67559",
      "termination_date": "20150316",
      "more_code_info": "",
      "recall_initiation_date": "20140127",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}