{
  "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": "San Diego",
      "address_1": "3978 Sorrento Valley Blvd Ste 300",
      "reason_for_recall": "Lack of Processing Controls: products produced in a manner that calls into question the sterility of the drug product intended to be sterile.",
      "address_2": "",
      "product_quantity": "191 vials",
      "code_info": "Lot #: 144326@3, Exp 07/10/2018; 145953@2, Exp 08/05/2018",
      "center_classification_date": "20180713",
      "distribution_pattern": "Product was distributed to patients via patient specific prescription only in CA.",
      "state": "CA",
      "product_description": "Glutathione 200mg/mL Injection w/Pres. (Benzyl Alcohol 1.5% in Sterile Water), 30 mL vial, Rx only, la VITA Compounding Pharmacy, 858.453.2500",
      "report_date": "20180725",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "La Vita Compounding Pharmacy, LLC",
      "recall_number": "D-0923-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "80416",
      "termination_date": "20190118",
      "more_code_info": "",
      "recall_initiation_date": "20180625",
      "postal_code": "92121-1436",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}