{
  "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": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65487",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "51 Valley Stream Pkwy",
      "address_2": "N/A",
      "postal_code": "19355",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "United States Nationwide Distribution in the states of ND, OH and SC.",
      "recall_number": "Z-1694-2013",
      "product_description": "Siemens Mammomat Inspiration -  full-field digital mammography    Product Usage:  Mammography",
      "product_quantity": "3",
      "reason_for_recall": "Firm became aware of an unintended behavior when using the Mammomat Inspiration.  The possibility exists that a malfunction may occur during Stereo or Tomo acquisitions if the tomo clutch was incorrectly adjusted.  Although the possibility is rare, the system could move while a patient's breast is compressed resulting in a possible bruise.  Firm released Update Instructions XP031/12/S for this iss",
      "recall_initiation_date": "20130228",
      "center_classification_date": "20130711",
      "termination_date": "20140221",
      "report_date": "20130717",
      "code_info": "Model number 10140000, serial numbers 3118, 3243 and 3309"
    }
  ]
}