{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Munich",
      "state": "N/A",
      "country": "Germany",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91781",
      "recalling_firm": "Brainlab AG",
      "address_1": "Olof-palme-str. 9",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Texas",
      "recall_number": "Z-1292-2023",
      "product_description": "Cirq Arm System 2.0",
      "product_quantity": "1 unit",
      "reason_for_recall": "Risk of mechanical instability due to potential manufacturing error of the device",
      "recall_initiation_date": "20230302",
      "center_classification_date": "20230328",
      "report_date": "20230405",
      "code_info": "56500 CIRQ ARM SYSTEM 2.0; GTIN 04056481143961; All available Serial numbers/lot numbers are affected."
    }
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}