{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Salt Lake City",
      "address_1": "605 N 5600 W",
      "reason_for_recall": "StatLockTM IV Premium Catheter Stabilization Device may contain an incorrectly sized retainer clip.",
      "address_2": "",
      "product_quantity": "4,500 units",
      "code_info": "Lot Number JUAQF675, Exp 2/28/2019",
      "center_classification_date": "20170519",
      "distribution_pattern": "Nationwide Distribution -  Internationally to Canada.       No govt/VA/Military consignees.",
      "state": "UT",
      "product_description": "StatLock¿ IV Premium Catheter Stabilization Device, product code IV0570.  sterile. Packaging:  packaged as single units in tyvek to film pouches, the product is distributed in cartons containing 25 devices and cases containing 250 devices.",
      "report_date": "20170531",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Bard Access Systems Inc.",
      "recall_number": "Z-2120-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77132",
      "termination_date": "20170821",
      "more_code_info": "",
      "recall_initiation_date": "20170425",
      "postal_code": "84116-3738",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}