{
  "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": "Terminated",
      "city": "Indiana",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "91263",
      "recalling_firm": "RemedyRepack Inc.",
      "address_1": "625 Kolter Dr Ste 4",
      "address_2": "N/A",
      "postal_code": "15701-3571",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was distributed to two different customers in MI.",
      "recall_number": "D-0077-2023",
      "product_description": "Desmopressin Acetate Tablet, 0.2 mg, 100-count box, Rx only, Source NDC: 23155-0490-01; MFG: Avet Pharmaceuticals Inc., East Brunswick, NJ  08816; Repackaged by: RemedyRepack Inc., Indiana, PA  15701, NDC #: 70518-3493-00.",
      "product_quantity": "9 boxes",
      "reason_for_recall": "Subpotent Drug: repackaged product was recalled by the manufacturer for subpotency.",
      "recall_initiation_date": "20221205",
      "center_classification_date": "20221207",
      "termination_date": "20230203",
      "report_date": "20221214",
      "code_info": "Lot # B1817019-082222, Exp. 02/24/2023; B1819127-082322, Exp. 02/26/2023"
    }
  ]
}