{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "San Clemente",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81743",
      "recalling_firm": "ICU Medical, Inc.",
      "address_1": "951 Calle Amanecer",
      "address_2": "N/A",
      "postal_code": "92673-6212",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.: CA, TX, WI, NY, NC, GA, PA, and NY.    Foreign: Canada",
      "recall_number": "Z-1071-2019",
      "product_description": "ICU Medical, Transpac IV Monitoring Kit With Safeset Reservoir and Blood Sampling Port, 60\" Tubing, Disposable Transducer, 3 ml Squeeze Flush, Macrodrip (Pole Mount), REF: 42640-06, Sterile EO",
      "product_quantity": "280",
      "reason_for_recall": "Reports of pressure tubing separation between the sampling port and the high pressure tubing on certain lots of extravascular blood pressure transducers, which could lead to delay in therapy, and in rare circumstances, pressure tubing separations could lead to blood loss, air embolism, or contamination of the fluid path.",
      "recall_initiation_date": "20181127",
      "center_classification_date": "20190328",
      "termination_date": "20220201",
      "report_date": "20190403",
      "code_info": "Lot/UDI:   3543099/ (01)0 0840619 04494 7 (17) 201001 (30) 01 (10) 3543099"
    }
  ]
}