{
  "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": [
    {
      "country": "United States",
      "city": "Vernon Hills",
      "address_1": "75 N Fairway Dr",
      "reason_for_recall": "The integrity of the sterile packaging is potentially compromised.",
      "address_2": "",
      "product_quantity": "4,240 units",
      "code_info": "Product Code: 4330  Lot Code:  0000837810; 0000840335; 0000842213; 0000848531; 0000851181; 0000853962",
      "center_classification_date": "20180418",
      "distribution_pattern": "Nationwide, Australia, Brazil, Canada, China, Japan, Kuwait, Malaysia, Mexico, Netherlands, New Zealand, Philippines, Singapore, South Africa, Taiwan, Thailand, United Arab Emirates, Vietnam",
      "state": "IL",
      "product_description": "Manometer, 550 ml three-Way Stopcock; STERILE;",
      "report_date": "20180425",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Carefusion 2200 Inc",
      "recall_number": "Z-1421-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76620",
      "termination_date": "20190709",
      "more_code_info": "",
      "recall_initiation_date": "20170223",
      "postal_code": "60061-1845",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}