{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Westborough",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97742",
      "recalling_firm": "Miach Orthopaedics",
      "address_1": "69 Milk St Ste 100",
      "address_2": "",
      "postal_code": "01581-1224",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-0479-2026",
      "product_description": "BEAR Implant (Bridge-Enhanced ACL Restoration);  Model/Catalog: 1000;",
      "product_quantity": "167 units",
      "reason_for_recall": "The field action was initiated in February of 2023 and was limited to the affected lot from sales force trunk stock only.",
      "recall_initiation_date": "20230202",
      "center_classification_date": "20251107",
      "report_date": "20251119",
      "code_info": "Model/Catalog: 1000; UDI-DI: 00860002987804;  Lot number: 7008409;",
      "more_code_info": ""
    }
  ]
}