{
  "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": "Center Valley",
      "address_1": "3773 Corporate Pkwy",
      "reason_for_recall": "The plastic sleeves of the Penis Clamp and Mouth Gag may stick together during or after reprocessing rendering the instruments unusable.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "OM040R",
      "center_classification_date": "20180411",
      "distribution_pattern": "nationwide",
      "state": "PA",
      "product_description": "Doyen-Collin Mouth Gag 120MM/ General Instruments",
      "report_date": "20180418",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Aesculap Implant Systems LLC",
      "recall_number": "Z-1358-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79656",
      "termination_date": "20200630",
      "more_code_info": "",
      "recall_initiation_date": "20180216",
      "postal_code": "18034-8217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}