{
  "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": "2026-07-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Navi Mumbai",
      "state": "N/A",
      "country": "India",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "99312",
      "recalling_firm": "Reliance Life Sciences Private Limited",
      "address_1": "Ttc Area Of Midc",
      "address_2": "R - 282 Dhirubhai Ambani Life Sciences Centre; Thane Belapur Road",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0672-2026",
      "product_description": "Pemetrexed for Injection 500mg/Vial, 1 50 mL Single-Dose Vial per carton, For intravenous use only, Rx only,  Manufactured for: Somerset Therapeutics, LLC., Somerset, NJ 08873 NDC: 70069-0835-01",
      "product_quantity": "5,020 vials",
      "reason_for_recall": "Lack of Sterility Assurance",
      "recall_initiation_date": "20260624",
      "center_classification_date": "20260708",
      "report_date": "20260715",
      "code_info": "Lot, expiry:            RPTH0125A Jan 31, 2028;   RPTH0225A Jan 31, 2028;   RPTH0325A Jan 31, 2028;   RPTH0725A Apr 30, 2028;"
    }
  ]
}