{
  "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": "2026-07-08",
    "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": "95128",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, Panama.",
      "recall_number": "Z-3116-2024",
      "product_description": "Medline convenience kits containing semi-rigid suction liners labeled as follows:  ANES TURNOVER KIT-LF, Pack Number DYNJAA10338J",
      "product_quantity": "1800 units",
      "reason_for_recall": "Due to reported adverse events, Medline Industries, LP. is issuing a recall on specific SKUs and lots of 1500 cc semi-rigid liners manufactured from 09/2023-11/2023 due to the potential loss of suction or low suction during intermittent suction use.",
      "recall_initiation_date": "20240627",
      "center_classification_date": "20240911",
      "report_date": "20240918",
      "code_info": "DYNJAA10338J:  UDI/DI case 40195327489695, UDI/DI each 10195327489694, Lot Numbers:  23LBO942, 24ABS046, 24BBS971",
      "more_code_info": ""
    }
  ]
}