{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99096",
      "recalling_firm": "Bard Access Systems, Inc.",
      "address_1": "605 N 5600 W",
      "address_2": "N/A",
      "postal_code": "84116-3738",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide U.S. Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, and WY. The country of Belgium.",
      "recall_number": "Z-2663-2026",
      "product_description": "CK000980A\tPowerMidline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741236150    P4254108\tPowerMidline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741129278    P4254108D\tPowerMidline Catheter 4 Fr Dual-Lumen  UDI-DI Code: 00801741129353      The PowerMidline\" Catheter is intended for short term peripheral access for selected intravenous therapies, blood sampling, and power injection of contrast media.",
      "product_quantity": "2,844",
      "reason_for_recall": "Due to lidocaine ampoules being manufactured under deficient manufacturing practices by manufacturer, lidocaine ampoules are currently being recalled by supplier.",
      "recall_initiation_date": "20260521",
      "center_classification_date": "20260702",
      "report_date": "20260708",
      "code_info": "CK000980A PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741236150 Lot Number: REKX0112  P4254108 PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129278 Lot Number: REKW0949  P4254108D PowerMidline Catheter 4 Fr Dual-Lumen UDI-DI Code: 00801741129353 Lot Number: REJZ1337"
    }
  ]
}