{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Beverly",
      "address_1": "50 Dunham Rd",
      "reason_for_recall": "The shears exhibited a high rate of complete or intermittent failure to actuate.  As a result, they do not perform their intended function in surgical procedures.",
      "address_2": "Suite 1500",
      "product_quantity": "115 units",
      "code_info": "UDI: 811099011439;  Lot Numbers: 807118, 807119, 807120, 811076",
      "center_classification_date": "20190531",
      "distribution_pattern": "The products were distributed to the following US states: ND and NY.    The products were distributed to the following foreign countries:  Germany, Netherlands.",
      "state": "MA",
      "product_description": "TLS2 Thermal Ligating Shears, Catalog Number 132-131D",
      "report_date": "20190612",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Microline Surgical, Inc.",
      "recall_number": "Z-1698-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82708",
      "termination_date": "20200730",
      "more_code_info": "",
      "recall_initiation_date": "20190322",
      "postal_code": "01915-1882",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}