{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lake Forest",
      "address_1": "275 N Field Dr",
      "reason_for_recall": "Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV administration sets.",
      "address_2": "",
      "product_quantity": "3,920,932 units in total",
      "code_info": "***** CANADA DISTRIBUTION *****     *** 1) List Number 14220-28-01",
      "center_classification_date": "20160629",
      "distribution_pattern": "US (Nationwide) Distribution",
      "state": "IL",
      "product_description": "*** 1) Product labeled in part: List No. 14220-28; PLUM Y-TYPE BLOOD SET; 200 Micron Filter, CLAVE Port, CLAVE Y-Site, Non-Vented, 110 Inch, Non-DEHP; Product  Usage:  The CLAVE of the secondary port is used as an easy secondary access that allows concurrent and piggyback mode in infusion. It is normally used with a syringe or a secondary IV infusion set.",
      "report_date": "20160706",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hospira Inc.",
      "recall_number": "Z-2060-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66372",
      "termination_date": "20161206",
      "more_code_info": "",
      "recall_initiation_date": "20130909",
      "postal_code": "60045-2579",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}