{
  "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": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94181",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "address_2": "N/A",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of MN and ND.  There as no foreign/military/government distribution.",
      "recall_number": "Z-1394-2024",
      "product_description": "IV Start Kit, containing 1 Saline Syringe 5ml, REF 74654, 100 kits/case, Sterile.",
      "product_quantity": "206,200 kits",
      "reason_for_recall": "The kits contain saline flush syringes which were recalled by the supplier.",
      "recall_initiation_date": "20240115",
      "center_classification_date": "20240328",
      "report_date": "20240403",
      "code_info": "Lot numbers 299477, 299849, 302983, 304173, 305500, 305501, 305514, 306363, 306683, 307030, 307809, 310701, 310887, 311741, 312807, and 313961;UDI-DI 10809160020388.",
      "more_code_info": ""
    }
  ]
}