{
  "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": {
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  "results": [
    {
      "country": "United States",
      "city": "Bedford",
      "address_1": "300 Northfield Rd",
      "reason_for_recall": "Lack of Assurance of Sterility: Crimp defects during visual inspection could affect container closure integrity.",
      "address_2": "",
      "product_quantity": "7172 vials",
      "code_info": "Lot # 0161-13-2167551; Exp. 07/14  Lot # 0161-13-2176919; Exp. 08/14",
      "center_classification_date": "20140818",
      "distribution_pattern": "Nationwide",
      "state": "OH",
      "product_description": "CYTARAbine for Injection USP, lyophiled in glass vials, 1 gram per vial, Rx only, Distributed by Bedford Laboratories, Bedford, OH 44146, Manufactured by Ben Venue Labs, Inc., Bedford, OH 44146, NDC 55390-808-01",
      "report_date": "20140827",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ben Venue Laboratories Inc",
      "recall_number": "D-1543-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "68800",
      "termination_date": "20141202",
      "more_code_info": "",
      "recall_initiation_date": "20140731",
      "postal_code": "44146-4650",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}