{
  "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": "Ongoing",
      "city": "Mason",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89176",
      "recalling_firm": "Haag-Streit USA Inc",
      "address_1": "3535 Kings Mills Rd",
      "address_2": "N/A",
      "postal_code": "45040-2303",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of OH, IN.",
      "recall_number": "Z-0478-2022",
      "product_description": "OCT-Camera 211 01 A3; Running software iOCT-Control 3 v1.4",
      "product_quantity": "3",
      "reason_for_recall": "Malfunction of the automatic laser beam shut-off, the OCT unit might not recognize whether the laser beam is safely switched off",
      "recall_initiation_date": "20211103",
      "center_classification_date": "20220110",
      "report_date": "20220119",
      "code_info": "Serial no. 0157, 0158 & 0171"
    }
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}