{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bensalem",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "88736",
      "recalling_firm": "SigmaPharm Laboratories LLC",
      "address_1": "3375 Progress Dr",
      "address_2": "N/A",
      "postal_code": "19020-5801",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0898-2021",
      "product_description": "Sodium Phenylbutyrate Powder, 250 Grams, Rx Only, packaged in 500 cc HDPE bottles and 53 mm CRC caps packed in a carton and then in case packs containing 2 bottles. Sigmapharm Laboratories, LLC, Bensalem, PA 19020, NDC 42794-086-14",
      "product_quantity": "1192 bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications; Out of Specification impurity results obtained during routine testing.",
      "recall_initiation_date": "20210921",
      "center_classification_date": "20210930",
      "termination_date": "20220926",
      "report_date": "20211006",
      "code_info": "Lots 2005401,  2005501, 2005601, 2005701, Exp FEB 2023; Lots 2101401, 2101501, Exp  FEB-2024"
    }
  ]
}