{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78575",
      "recalling_firm": "Medline Industries Inc",
      "address_1": "Three Lakes Drive",
      "address_2": "",
      "postal_code": "60093",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide USA, Puerto Rico, China, Chile, Guam, Honduras, India, Israel, Malaysia, Mexico, Turkey",
      "recall_number": "D-0314-2018",
      "product_description": "Medline Skin Stapler RMVR, Tray  Sterile, Single Use Only. Packaged in Mexico for Medline Industries, Inc., Mundelein, IL 60060",
      "product_quantity": "592 ases",
      "reason_for_recall": "Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads  is below label claim of 0.85%.",
      "recall_initiation_date": "20170921",
      "center_classification_date": "20180204",
      "termination_date": "20230828",
      "report_date": "20180207",
      "code_info": "Pack Number: P888937; Lots 177B0658; 17QB8268  Pack Number: P888937H; Lots 17QB8268",
      "more_code_info": ""
    }
  ]
}