{
  "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": "2026-03-18",
    "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": "91483",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-1124-2023",
      "product_description": "Surgical convenience kits labeled as:   a)  CENTURION MEDICAL PRODUCTS CENTRAL LINE DRESSING CHANGE K, Reorder Number DT21400;   b)  CENTURION MEDICAL PRODUCTS CUSTOM PORT ACCESS KIT, Reorder Number DT22255;    c)  MEDLINE CVC DRESSING CHANGE KIT, Reorder Number DYNDC1022GB,",
      "product_quantity": "1588 units",
      "reason_for_recall": "The recall is due to the perforated bag not allowing for outside of the kit wrapping to be sterile, therefore, only the contents inside the kits wrapping are sterile.",
      "recall_initiation_date": "20221207",
      "center_classification_date": "20230210",
      "report_date": "20230222",
      "code_info": "a)  Reorder Number DT21400, GTIN 40653160318225 Lot # 22HMH962;  b)  Reorder Number DT22255, GTIN 40653160328644 Lot # 22HMH427;  c)  Reorder Number DYNDC1022GB, GTIN 40195327038701 Lot # 22GBY236"
    }
  ]
}