{
  "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": "95127",
      "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": "E-Mail",
      "distribution_pattern": "US:  TX, IL, CA",
      "recall_number": "Z-3072-2024",
      "product_description": "ANESTHESIA TURNOVER KIT, Pack Number DYNJAA0377A",
      "product_quantity": "315 units",
      "reason_for_recall": "A non-sterile Mastisol component, which was not labeled as being sterile or non-sterile, was placed in the non-sterile portion of certain sterile convenience kits and distributed.  In the event that the user assumes sterility during its use, there is an increased risk of patient infection.",
      "recall_initiation_date": "20240618",
      "center_classification_date": "20240906",
      "report_date": "20240918",
      "code_info": "UDI/DI Case 40195327334209, UDI/DI Each 10195327334208; Lot Numbers:  23IBJ309, 23GBA500, 23GBA457, 23CBE394, 23BBL312",
      "more_code_info": ""
    }
  ]
}