{
  "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": "Boerne",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86797",
      "recalling_firm": "Prytime Medical Devices, Inc.",
      "address_1": "229 N Main St",
      "address_2": "N/A",
      "postal_code": "78006-2035",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of Utah.",
      "recall_number": "Z-0716-2021",
      "product_description": "PryTime Medical - ER-Reboa Plus Catheter, Ref: ER7232PLUS, Guidewire Free, Compatabel with 7Fr introducer Sheaths, Arterial Line, Rx Only, UDI: (01) 0 0850001 10505 7 - Product Usage: intended for temporary occlusion of large vessels and blood pressure monitoring including patients requiring emergency control of hemorrhage.",
      "product_quantity": "3 units",
      "reason_for_recall": "There is a potential that  catheters may have incorrectly marked balloon  and arterial lines.  This could result in a  procedure  delay or injury to the patient.",
      "recall_initiation_date": "20201029",
      "center_classification_date": "20201223",
      "termination_date": "20230111",
      "report_date": "20201230",
      "code_info": "Lot # 205936"
    }
  ]
}