{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Terminated",
      "city": "San Diego",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89778",
      "recalling_firm": "Adamis Pharmaceuticals Corporation",
      "address_1": "11682 El Camino Real Ste 300",
      "address_2": "",
      "postal_code": "92130-2092",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide in the U.S.A.",
      "recall_number": "D-0764-2022",
      "product_description": "SYMJEPI (epinephrine injection, USP) 0.15 mg (0.15 mg/0.3 mL), Two Pre-Filled Single-Dose Syringes per carton, Rx Only, Manufactured for Adamis Pharmaceuticals Corp.; San Diego, CA  92130; Distributed by USWM, LLC., Louisville, KY  40241, Made in Belgium, NDC 78670-131-02.",
      "product_quantity": "2,500 cartons",
      "reason_for_recall": "Defective Delivery System: Potential clogging of the needle preventing the dispensing of epinephrine.",
      "recall_initiation_date": "20220321",
      "center_classification_date": "20220408",
      "termination_date": "20230208",
      "report_date": "20220413",
      "code_info": "Lot # 21101Y, Exp. 11/30/2022",
      "more_code_info": ""
    }
  ]
}