{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Ledgewood",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "93160",
      "recalling_firm": "Imprimis NJOF, LLC",
      "address_1": "1705 Route 46 Ste 6B",
      "address_2": "N/A",
      "postal_code": "07852-9720",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0040-2024",
      "product_description": "Epinephrine-Lidocaine HCl (0.25mg/mL and 7.5mg/mL) 1mL Single Use Intraocular injection Preservative Free NDC 71384-640-01  Not for resale. Office use only. Lot: 23APR018 Date Compounded: 24APR2023  Expires on: 17APR2024. In case of adverse event contact: www.fda.gov/medwatch or (800)-FDA-1088 Imprimis NJOF, LLC. 1705 Route 46 West, Unit 6B, Ledgewood, NJ, 07852 (844) 446-6979",
      "product_quantity": "364 bags (1 mL filled in 2 mL glass amber vials; 20 vials shipped in a bag)",
      "reason_for_recall": "Subpotent: Failing Test Results for Epinephrine",
      "recall_initiation_date": "20231003",
      "center_classification_date": "20231005",
      "termination_date": "20250321",
      "report_date": "20231011",
      "code_info": "23APR018"
    }
  ]
}