{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Indiana",
      "address_1": "625 Kolter Dr Ste 4",
      "reason_for_recall": "Failed pH Specifications: High Out-of-Specification results for pH were obtained during stability testing.",
      "address_2": "",
      "product_quantity": "1 vial",
      "code_info": "Lot #: A0A0253, Exp. 02/2019; Lot #: B0369427-112717, Exp. 08/2019",
      "center_classification_date": "20181114",
      "distribution_pattern": "1 vial was distributed to a medical facility in Mayville, NY.",
      "state": "PA",
      "product_description": "Metoprolol Tartrate Injection, USP 5mg/5mL, vials, Rx only, MFG: Claris Lifesciences Inc., North Brunswick, NJ 08902, NDC# 70518-0868-00",
      "report_date": "20181121",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "RemedyRepack Inc.",
      "recall_number": "D-0245-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "81554",
      "termination_date": "20190205",
      "more_code_info": "",
      "recall_initiation_date": "20181026",
      "postal_code": "15701-3571",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}