{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allegan",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "M013"
        ],
        "brand_name": [
          "INFANTS PAIN AND FEVER"
        ],
        "generic_name": [
          "ACETAMINOPHEN"
        ],
        "manufacturer_name": [
          "Kroger Company"
        ],
        "product_ndc": [
          "30142-766"
        ],
        "product_type": [
          "HUMAN OTC DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "ACETAMINOPHEN"
        ],
        "rxcui": [
          "307668"
        ],
        "spl_id": [
          "2a7339bd-2db6-45a5-bbe0-cf55df3154fd"
        ],
        "spl_set_id": [
          "7dbe284a-c0d5-4ac4-8445-611610f3c0fb"
        ],
        "package_ndc": [
          "30142-766-16"
        ],
        "is_original_packager": [
          true
        ],
        "unii": [
          "362O9ITL9D"
        ]
      },
      "product_type": "Drugs",
      "event_id": "88905",
      "recalling_firm": "Perrigo Company PLC",
      "address_1": "515 Eastern Ave",
      "address_2": "",
      "postal_code": "49010-9070",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0596-2022",
      "product_description": "Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202.  NDC: 30142-766-16",
      "product_quantity": "5,184 bottles",
      "reason_for_recall": "CGMP Deviations: Products were manufactured with contaminated excipient that was recalled from the excipient supplier.",
      "recall_initiation_date": "20211026",
      "center_classification_date": "20220223",
      "termination_date": "20230929",
      "report_date": "20220302",
      "code_info": "Batch: 1CK1274, Exp 02/28/2023",
      "more_code_info": ""
    }
  ]
}