{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "47262",
      "product_res_number": "Z-0030-2007",
      "event_date_initiated": "2006-06-20",
      "event_date_posted": "2006-10-12",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-10-16",
      "res_event_number": "35959",
      "product_code": "NVM",
      "product_description": "Arrow Double-Lumen Balloon Wedge Pressure Catheter, for sampling blood for oxygen levels and measuring pressures in the right heart.",
      "code_info": "MF5124329",
      "firm_fei_number": "3015859709",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "city": "Reading",
      "state": "PA",
      "postal_code": "19605-9607",
      "additional_info_contact": "Terrance M. Larkin\n610-378-0131",
      "reason_for_recall": "The print identifying the two extension lines, CVP Proximal and PA Distal, are reversed.",
      "root_cause_description": "Other",
      "action": "Recall letter was sent to customers on 6/20/2006 by US mail.",
      "product_quantity": "11 units",
      "distribution_pattern": "Medical facilities located in MD, IL, MO, MA and United Kingdom, for a total of 5.",
      "openfda": {
        "k_number": [
          "K160889",
          "K161451",
          "K213915",
          "K050857",
          "K211134"
        ],
        "registration_number": [
          "3005706667",
          "1318694",
          "2528981"
        ],
        "fei_number": [
          "3005706667",
          "1318694",
          "2528981"
        ],
        "device_name": "Catheter, Angioplasty, Peripheral, Transluminal, Dual-Balloon",
        "medical_specialty_description": "Cardiovascular",
        "regulation_number": "870.1250",
        "device_class": "2"
      }
    }
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}