{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Arden",
      "address_1": "25 Heywood Rd",
      "reason_for_recall": "Some of the sterile kits may have incomplete seals which might compromise the sterility of the kits.",
      "address_2": "",
      "product_quantity": "474 cs (9,480 ea) total for all kits involved",
      "code_info": "Model number: 72347, Lot number: 187172, Exp. Date: 9/1/2015.",
      "center_classification_date": "20140701",
      "distribution_pattern": "Distributed in the states of AR, AZ, FL, GA, IA, IL, KY, MA, MN, NC, NY, OH, TN, TX, and VA.",
      "state": "NC",
      "product_description": "Laceration/Suture Removal, Sterile Single Use, Latex Free, 20/case, Medical Action Industries, Inc, Arden, NC.",
      "report_date": "20140709",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medical Action Industries Inc",
      "recall_number": "Z-1951-2014",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "68564",
      "termination_date": "20150203",
      "more_code_info": "",
      "recall_initiation_date": "20140612",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}