{
  "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": "Ongoing",
      "city": "Chicago",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA214540"
        ],
        "brand_name": [
          "CETRORELIX ACETATE"
        ],
        "generic_name": [
          "CETRORELIX ACETATE"
        ],
        "manufacturer_name": [
          "Meitheal Pharmaceuticals Inc."
        ],
        "product_ndc": [
          "71288-558"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "SUBCUTANEOUS"
        ],
        "rxcui": [
          "283402"
        ],
        "spl_id": [
          "1f143808-6446-45a1-9a8c-9e58a26c22cb"
        ],
        "spl_set_id": [
          "9b3057ac-6cac-4509-a355-df76247b992c"
        ],
        "package_ndc": [
          "71288-558-90",
          "71288-556-02",
          "71288-557-81"
        ],
        "is_original_packager": [
          true
        ]
      },
      "product_type": "Drugs",
      "event_id": "98386",
      "recalling_firm": "Meitheal Pharmaceuticals, Inc",
      "address_1": "8700 W Bryn Mawr Ave Ste 600s",
      "address_2": "N/A",
      "postal_code": "60631-3529",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide",
      "recall_number": "D-0340-2026",
      "product_description": "Cetrorelix Acetate for Injection (Kit), 0.25 mg per vial, Single-Dose Kit, Rx Only, Mfd. for: Meitheal Pharmaceuticals, Chicago, IL  NDC 71288-558-90.",
      "product_quantity": "16,477 kits",
      "reason_for_recall": "Defective Delivery System: Missing or duplicated needles within the injection kit",
      "recall_initiation_date": "20260209",
      "center_classification_date": "20260223",
      "report_date": "20260218",
      "code_info": "Lot Q4E0112A, Exp.: 30 Apr 2027"
    }
  ]
}