{
  "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,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Rochester",
      "state": "MI",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "94166",
      "recalling_firm": "Par Sterile Products LLC",
      "address_1": "870 Parkdale Rd",
      "address_2": "N/A",
      "postal_code": "48307-1740",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0429-2024",
      "product_description": "Treprostinil Injection, 20 mg/20 mL (1 mg/mL), For Subcutaneous or Intravenous Infusion Only, 20 mL Multiple-Dose Vial, Rx Only, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977.  NDC: 42023-206-01",
      "product_quantity": "466 vials",
      "reason_for_recall": "Presence of Particulate Matter.",
      "recall_initiation_date": "20240304",
      "center_classification_date": "20240328",
      "report_date": "20240403",
      "code_info": "Lot#: 57014; Exp, 04/30/2024",
      "more_code_info": ""
    }
  ]
}