{
  "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": "Tuttlingen",
      "state": "",
      "country": "Germany",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80970",
      "recalling_firm": "Dannoritzer Medizintechnik GmbH & Co. KG",
      "address_1": "Sattlerstr. 25",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide in the States of OH, MI, MA, CA, OK, TN, GA, FL, IL, NC, TX, MO.",
      "recall_number": "Z-0062-2019",
      "product_description": "Laparoscopy Instruments Instructions For Use (IFU) for the following: 1)Monopolar electrode, 2) Insert, handle and/or shaft component of a modular forceps or scissors for electrosurgical coagulation, 3) One-piece forceps or scissors for electrosurgical coagulation",
      "product_quantity": "",
      "reason_for_recall": "The Manual cleaning process and the usability of the reprocessing instruction by the user had not been validated.  The IFU was modified to remove the manual cleaning method and revised the instructions for use for clarity and readability.",
      "recall_initiation_date": "20180806",
      "center_classification_date": "20181003",
      "termination_date": "20190722",
      "report_date": "20181010",
      "code_info": "none",
      "more_code_info": ""
    }
  ]
}