{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Salt Lake City",
      "state": "UT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88057",
      "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": "U.S. Nationwide distribution in the state of RI.",
      "recall_number": "Z-1994-2021",
      "product_description": "5 Fr IR PowerPICC Convenience Kit Catheter Dual Lumen with 70 cm Guidewire    Unit Label:  PowerPICC REF CK000340B  BARD MYPICC KIT 5F French Size Dual-Lumen 70cm Guidewire",
      "product_quantity": "30 kits",
      "reason_for_recall": "Catheter convenience kits contain the incorrect guidewire. Kits were labeled with 70cm guidewires, but contained a 50cm guidewire.",
      "recall_initiation_date": "20210519",
      "center_classification_date": "20210701",
      "termination_date": "20230331",
      "report_date": "20210707",
      "code_info": "Catalog (REF) Number: CK000340B  UDI Code: (01)00801741126697  Lot Number: 20BBK658"
    }
  ]
}