{
  "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": [
    {
      "country": "United States",
      "city": "Shirley",
      "address_1": "One Luitpold Drive",
      "reason_for_recall": "Presence of Particulate Matter",
      "address_2": "P.O. Box 9001",
      "product_quantity": "63,750 ampules",
      "code_info": "Lot #1395 Exp: July 2012",
      "center_classification_date": "20120716",
      "distribution_pattern": "Nationwide",
      "state": "NY",
      "product_description": "Epinephrine Injection, USP, 1:1000 (1 mg/mL), 25 x 1 mL Ampules, For SC and IM Use, For IV and IC Use after Dilution,  Rx Only, American Regent, Inc., Shirely, NY 11967 --NDC 0517-1071-25",
      "report_date": "20120725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Luitpold Pharmaceuticals, Inc.",
      "recall_number": "D-1421-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "61714",
      "termination_date": "20170411",
      "more_code_info": "",
      "recall_initiation_date": "20120424",
      "postal_code": "11967-9001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}