{
  "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": "Rocky Mount",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77533",
      "recalling_firm": "Hospira a Pfizer Company",
      "address_1": "4285 N Wesleyan Blvd",
      "address_2": "N/A",
      "postal_code": "27804-8612",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
      "distribution_pattern": "U.S. (including Puerto Rico), Dutch Antilles, Barbados, Canada, Philippines, Kuwait, and Singapore",
      "recall_number": "D-1049-2017",
      "product_description": "Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only, Mfd by Hospira, INC, Lake Forest, IL 60045 USA",
      "product_quantity": "21,436,700 5mL single dose vials",
      "reason_for_recall": "Lack of Sterility Assurance",
      "recall_initiation_date": "20170615",
      "center_classification_date": "20170801",
      "termination_date": "20200720",
      "report_date": "20170809",
      "code_info": "a.) one vial:    Lot: 72226EV Exp. 12/01/2018  Lot: 72236EV Exp. 12/01/2018  Lot: 75382EV Exp. 03/01/2019   Lot: 75383EV Exp. 03/01/2019    b.) 25 vial carton:    Lot: 7538EV; Exp 03/01/2019"
    }
  ]
}