{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Richmond",
      "state": "VA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79341",
      "recalling_firm": "Cypress Medical Products LLC",
      "address_1": "9954 Mayland Dr Ste 4000",
      "address_2": "N/A",
      "postal_code": "23233-1464",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to states of: CO, FL, GA, KY, MI, MO, NC, NH, OH, TN, TX, WA, AND WI.",
      "recall_number": "Z-0932-2018",
      "product_description": "241-McKesson Premium Skin Staple Remover Kit, Item #100123, McKesson I.V. Start Kit, 100124-McKesson Suture Removal Kit, and 82-15 Cypress Medical Products Skin Staple Remover Kit. McKesson Item # 241, 100123, and 100124, Cypress Item # 82-15     Manual surgical instrument for general use.",
      "product_quantity": "12,206 cases",
      "reason_for_recall": "Product not meeting the iodine assay level requirements to support 36 month expiration dating.",
      "recall_initiation_date": "20171117",
      "center_classification_date": "20180308",
      "termination_date": "20200408",
      "report_date": "20180314",
      "code_info": "Item   241, 100123, 100124, 82-15"
    }
  ]
}