{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allegan",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "M013"
        ],
        "brand_name": [
          "UP AND UP ACETAMINOPHEN"
        ],
        "generic_name": [
          "ACETAMINOPHEN"
        ],
        "manufacturer_name": [
          "Target Corporation"
        ],
        "product_ndc": [
          "11673-133"
        ],
        "product_type": [
          "HUMAN OTC DRUG"
        ],
        "route": [
          "ORAL"
        ],
        "substance_name": [
          "ACETAMINOPHEN"
        ],
        "rxcui": [
          "307668"
        ],
        "spl_id": [
          "af4a4454-2cfd-4d5a-93ce-54c0437ccb62"
        ],
        "spl_set_id": [
          "c1dd8330-fb6b-4d1f-9484-c199dc69214d"
        ],
        "package_ndc": [
          "11673-133-16",
          "11673-133-26"
        ],
        "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-0584-2022",
      "product_description": "Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml), 2 FL OZ (59 mL) per bottle, Distributed by Target Corporation, Minneapolis, MN 55403.  NDC: 11673-133-16",
      "product_quantity": "22,140 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: 1CK0907, Exp 01/31/2023",
      "more_code_info": ""
    }
  ]
}