{
  "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": [
    {
      "status": "Terminated",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80702",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "Three Lakes Drive",
      "address_2": "N/A",
      "postal_code": "60093",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution to states of: CA, CT, DE, FL, GA, IN, LA, MA, MD, MN, MS, NC, NJ, NM, NY, OH, OK, OR, PA, RI, SC, TN, TX, VA, VT, WA and WV",
      "recall_number": "Z-2948-2018",
      "product_description": "Medline 0.9 % Sodium Chloride Injection, USP   5 mL in 10 mL Syringe ZR       Intended for flushing IV catheters and IV tubing only.",
      "product_quantity": "90,870 units",
      "reason_for_recall": "Packaged with an incorrect overwrap.",
      "recall_initiation_date": "20180201",
      "center_classification_date": "20180829",
      "termination_date": "20201005",
      "report_date": "20180905",
      "code_info": "Lot # 3131591"
    }
  ]
}