{
  "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": "2026-10-14",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Madurai",
      "state": "",
      "country": "India",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "M018"
        ],
        "brand_name": [
          "FOCUS PI"
        ],
        "generic_name": [
          "HYPROMELLOSE EYE DROPS 0.7%"
        ],
        "manufacturer_name": [
          "COVALENT MEDICAL"
        ],
        "product_ndc": [
          "82724-007"
        ],
        "product_type": [
          "HUMAN OTC DRUG"
        ],
        "route": [
          "OPHTHALMIC"
        ],
        "substance_name": [
          "HYPROMELLOSE 2910 (4000 MPA.S)"
        ],
        "rxcui": [
          "2743251"
        ],
        "spl_id": [
          "7d464072-62dd-4b68-8558-9008989000ad"
        ],
        "spl_set_id": [
          "e9b2afdd-049a-3987-e053-2a95a90a6cbb"
        ],
        "package_ndc": [
          "82724-007-19"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "RN3152OP35"
        ]
      },
      "product_type": "Drugs",
      "event_id": "99903",
      "recalling_firm": "Aurolab Trust",
      "address_1": "1 Sivagangai Main Road",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "VA",
      "recall_number": "D-0874-2026",
      "product_description": "FOCUS PI Hypromellose 0.7% Formula, 0.3 FL O (10 mL) per vial, STERILE, Manufactured for: Covalent Management, Inc., Manassas, VA 20109.  NDC: 82724-007-19",
      "product_quantity": "25,220 bottles",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20260917",
      "center_classification_date": "20260928",
      "report_date": "20261007",
      "code_info": "Batch# 6B093FI, Exp. 04/01/28; Batch# 6F511F1, Exp. 05/15/28",
      "more_code_info": ""
    }
  ]
}