{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "South San Francisco",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78088",
      "recalling_firm": "Genentech, Inc.",
      "address_1": "1 Dna Way",
      "address_2": "N/A",
      "postal_code": "94080-4990",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-1175-2017",
      "product_description": "Activase (alteplase), 100 mg (58 million IU), Lyophilized vial, packaged with 1 single-dose 100ml vial of sterile water for Injection USP and one transfer device.  Manufactured by: Genentech, Inc. 1 DNA Way, South San Francisco, CA 84080-4990. NDC: 50242-0085-27",
      "product_quantity": "16,882",
      "reason_for_recall": "Non-Sterility:presence of cracked or chipped glass at the neck of Sterile Water for Injection vials.",
      "recall_initiation_date": "20170905",
      "center_classification_date": "20171201",
      "termination_date": "20190111",
      "report_date": "20170927",
      "code_info": "Lot# 3128243, 3141239, EXP. 9/30/2018; 3166728, EXP. 2/28/2019.",
      "more_code_info": ""
    }
  ]
}