{
  "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": "89331",
      "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 one direct account in PA.",
      "recall_number": "D-0366-2022",
      "product_description": "Metformin 750 mg Extended Release  NDC # 70518-2920-00",
      "product_quantity": "56 Blister Cards",
      "reason_for_recall": "CGMP Deviations: Detection of N-Nitrosodimethylamine (NDMA) levels in excess of the Acceptable Daily Intake Limit.",
      "recall_initiation_date": "20211230",
      "center_classification_date": "20220111",
      "termination_date": "20220328",
      "report_date": "20220119",
      "code_info": "Lot #  J0511265-021121, exp. date 02/28/2022   J0499451-122220, exp. date 01/31/2022   J0496563-120820, exp. date 12/31/2021   J0495111-120120, exp. date 12/31/2021"
    }
  ]
}