{
  "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": "2026-09-16",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99613",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "address_2": "",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US distribution to states of: IA, VA, MO, KS, FL, OH and LS.",
      "recall_number": "Z-3106-2026",
      "product_description": "Kit: Epidural/Pain TQC 20/Cs, REF: 82465 Containing Sodium Chloride Injection, 0.9%, USP 10ml ampules",
      "product_quantity": "1,960",
      "reason_for_recall": "Kits containing Sodium Chloride ampules subject to another recall are recalled due to potentially compromised sterility.",
      "recall_initiation_date": "20260723",
      "center_classification_date": "20260909",
      "report_date": "20260916",
      "code_info": "UDI-DI: 10809160367414. Lot(Expiration Date): 322200(4/1/2026), 324586(4/1/2026), 327335(4/1/2026), 329618(9/1/2026), 347199(11/1/2026), 337283(11/1/2026), 350354(11/30/2026), 375449(5/31/2027)",
      "more_code_info": ""
    }
  ]
}