{
  "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": [
    {
      "country": "United States",
      "city": "Waukegan",
      "address_1": "1500 S Waukegan Rd",
      "reason_for_recall": "Product's seal possibly compromised, potentially compromising the sterility of the package contents.  Use of impacted products could result in an increased risk of infection.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Catalog Number: SU130-1310  Lot Numbers:  1161230  1161231  1161232  1161233  1161234  1161398  1161399  1161400  1161401  1161402  1161403  1161404  1161492  1161493  1161494  1161495  1161496  1161497  1161498  1161499  1161614  1161615  1161616  1161617  1170076  1170077  1170080",
      "center_classification_date": "20170523",
      "distribution_pattern": "Nationwide Distribution",
      "state": "IL",
      "product_description": "Jackson-Pratt Silicone Flat Drain, 7mm, Full Ducts. Sterile, Rx Only.  For Single Use Only.   Jackson-Pratt Wound Drainage Systems are sterile single use devices. The wound drainage system consist of a wound drain and a fluid collection reservoir. The wound drain is a radio-opaque section of tubing which has perforations or ducts. The wound drain is surgically placed in a surgical wound site using a trocar. Blood and fluids are collected through a wound drain into a fluid collection reservoir. Wound drains are used to remove exudates from wound sites. Trocars, drains and reservoirs are for a single patient use only and should be discarded after use",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Cardinal Health 200, LLC",
      "recall_number": "Z-2143-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77127",
      "termination_date": "20171227",
      "more_code_info": "",
      "recall_initiation_date": "20170421",
      "postal_code": "60085-6728",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}