{
  "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": "Bryan",
      "address_1": "705 E Mulberry St",
      "reason_for_recall": "Failed Dissolution Specifications",
      "address_2": "",
      "product_quantity": "2839 bottles",
      "code_info": "BZP0093A, BZP0094A, BZP0095A, BZP0096A, BZP0097A, Exp 02/2017",
      "center_classification_date": "20160614",
      "distribution_pattern": "Nationwide",
      "state": "OH",
      "product_description": "Nitrofurantoin Oral Suspension, USP, 25 mg/5 mL, FOR ORAL USE ONLY, URINARY TRACT ANTIBACTERIAL, Rx Only , 240 mL bottle, Dist. by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, Mfg. by: Sun Pharmaceutical Industries, Inc., Bryan, Ohio 43506, NDC 57664-239-32",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Nostrum Laboratories, Inc.",
      "recall_number": "D-1030-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "74194",
      "termination_date": "20170428",
      "more_code_info": "",
      "recall_initiation_date": "20160523",
      "postal_code": "43506-1432",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}