{
  "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: SU130-1311  Lot Numbers:  1161247  1161248  1161249  1161250  1161251  1161252  1161414  1161415  1161416  1161417  1161418  1161419  1161420  1161421  1161509  1161510  1161511  1161512  1161513  1161514  1161515  1161622  1161623  1161624  1161625  1161626  1161627  1161628  1170089  1170094  1170095  1170096  1170353  1170354  1170356",
      "center_classification_date": "20170523",
      "distribution_pattern": "Nationwide Distribution",
      "state": "IL",
      "product_description": "Jackson-Pratt Silicone Flat Drain, 10mm, 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-2144-2017",
      "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"
    }
  ]
}