{
  "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-2662-2026",
      "product_description": "CK000727\tPowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741138478    CK000729\tPowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741138713    P4153108D\tPowerMidline Catheter 3 Fr Single-lumen  UDI-DI Code: 00801741108747    P4154108\tPowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108754    P4154108D\tPowerMidline Catheter 4 Fr Single-Lumen  UDI-DI Code: 00801741108761      The PowerMidline\" Catheter is intended for short term peripheral access for selected intravenous therapies, blood sampling, and power injection of contrast media.",
      "product_quantity": "16,887",
      "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": "CK000727 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138478 Lot Numbers: REKP2822 REKW2840 REKX3882  CK000729 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741138713 Lot Number:  REKW2434  P4153108D PowerMidline Catheter 3 Fr Single-lumen UDI-DI Code: 00801741108747 Lot Number: REKW0907  P4154108 PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108754 Lot Numbers: REKW2479 REKX3439  P4154108D PowerMidline Catheter 4 Fr Single-Lumen UDI-DI Code: 00801741108761 Lot Numbers: REKP0895 REKX0665 REKX2216 REKY1281"
    }
  ]
}