{
  "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": "East Brunswick",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82198",
      "recalling_firm": "Heritage Pharmaceuticals, Inc.",
      "address_1": "1 Tower Center Blvd Ste 1700",
      "address_2": "N/A",
      "postal_code": "08816-1145",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-1065-2019",
      "product_description": "Etomidate Injection, USP 20 mg/10mL (2mg/mL) 10 mL Single-Dose Vial, Rx only, Manufactured for: Heritage Pharmaceuticals Inc. Made in India, NDC 23155-160-31",
      "product_quantity": "11888 units",
      "reason_for_recall": "Subpotent Drug.",
      "recall_initiation_date": "20190215",
      "center_classification_date": "20190327",
      "termination_date": "20210304",
      "report_date": "20190327",
      "code_info": "Lot #: AMA701, Exp. March 2019; AMA702, AMA703, Exp August 2019."
    }
  ]
}