{
  "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,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mukilteo",
      "state": "WA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
        "application_number": [
          "ANDA090963"
        ],
        "brand_name": [
          "GLYCOPYRROLATE"
        ],
        "generic_name": [
          "GLYCOPYRROLATE"
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        "manufacturer_name": [
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        ],
        "product_ndc": [
          "51662-1487"
        ],
        "product_type": [
          "HUMAN PRESCRIPTION DRUG"
        ],
        "route": [
          "INTRAMUSCULAR",
          "INTRAVENOUS"
        ],
        "substance_name": [
          "GLYCOPYRROLATE"
        ],
        "rxcui": [
          "1731582"
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        "spl_id": [
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        ],
        "spl_set_id": [
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        "package_ndc": [
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          "51662-1487-2",
          "51662-1487-3"
        ],
        "original_packager_product_ndc": [
          "0143-9682"
        ],
        "unii": [
          "V92SO9WP2I"
        ]
      },
      "product_type": "Drugs",
      "event_id": "92468",
      "recalling_firm": "HF Acquisition Co LLC",
      "address_1": "11629 49th Pl W",
      "address_2": "",
      "postal_code": "98275-4255",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distributed in TX, AZ and CA only",
      "recall_number": "D-0870-2023",
      "product_description": "GLYCOPYRROLATE INJECTION, USP 0.2MG/ML, 1mL VIAL, manufactured by HF Acquisition Co. LLC, Mukilteo, WA 98275, NDC 51662-1487-3",
      "product_quantity": "9 boxes of 25 vials",
      "reason_for_recall": "Labeling: Label Mix-up",
      "recall_initiation_date": "20230606",
      "center_classification_date": "20230608",
      "termination_date": "20240227",
      "report_date": "20230614",
      "code_info": "Lot #: 2205095.1, Exp. Date 7/31/2024",
      "more_code_info": ""
    }
  ]
}