{
  "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": "Amityville",
      "state": "NY",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "66675",
      "recalling_firm": "Hi-Tech Pharmacal Co., Inc.",
      "address_1": "369 Bayview Ave",
      "address_2": "N/A",
      "postal_code": "11701-2801",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-389-2014",
      "product_description": "Acyclovir Oral Suspension, USP 200 mg/5 mL, Net Wt. 16 fl oz (473 mL), Rx only, Hi-Tech Pharmacal Co, Inc. Amityville, NY 11701.  NDC 50383-810-16.",
      "product_quantity": "51.948 bottles",
      "reason_for_recall": "Failed Stability Specification; product viscosity and or pH are below specification.",
      "recall_initiation_date": "20131028",
      "center_classification_date": "20131224",
      "termination_date": "20160516",
      "report_date": "20140101",
      "code_info": "Batch no: 1) 614463 (exp. 03/2014),  2) 612905 (exp. 12/2013), 3) 614923 (exp. 03/2014), 4) 615852 (exp. 05/2014), 5) 615855 (exp. 05/2014), 6) 616689 (exp. 07/2014), 7) 616692 (exp. 07/2014).",
      "more_code_info": ""
    }
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}