{
  "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": "2026-10-21",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99888",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of AZ, CA, IN, MD, MO, NJ, OH, and WI.",
      "recall_number": "Z-0184-2027",
      "product_description": "Convenience Kits containing CONMED AirSeal Access Ports    ADVANCE LAPAROSCOPIC\t  \tDYNJ911135A  \t  CHN GYN ONCOLOGY\t  \tDYNJ906731M",
      "product_quantity": "3,551 kits",
      "reason_for_recall": "Kits contain CONMED AirSeal Access Ports. The ports were recalled by manufacturer due to potential for erroneous overpressure alerts and system venting during use, which may result in delays or ending procedures.",
      "recall_initiation_date": "20260831",
      "center_classification_date": "20261015",
      "report_date": "20261021",
      "code_info": "DYNJ911135A    UDI-DI 10198459655623    Lot 26EDA606    DYNJ906731M    UDI-DI 10198459567117    Lots 25KDA658   25KDB571   25LDB411   26CDA536",
      "more_code_info": ""
    }
  ]
}