{
  "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": {
      "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": "83415",
      "recalling_firm": "Siemens Medical Solutions USA, Inc",
      "address_1": "40 Liberty Blvd",
      "address_2": "N/A",
      "postal_code": "19355-1418",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "AL  AR  AZ  CA  CO  CT  DC  DE  FL  GA  GU  IA  ID  IL  IN  KS  KY  LA  MA  MD  ME  MI  MN  MO  MT  NC  NE  NH  NJ  NY  OH  OK  OR  PA  SC  TN  TX  VA  WA  WI  WV  WY",
      "recall_number": "Z-2342-2019",
      "product_description": "MAGNETOM Aera magnetic resonance diagnostic devices   Model # 10432914",
      "product_quantity": "143",
      "reason_for_recall": "Potential of an open port in the quench venting system when using the optional horizontal outlet on the quench line assembly.",
      "recall_initiation_date": "20190709",
      "center_classification_date": "20190822",
      "termination_date": "20200423",
      "report_date": "20190828",
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}