{
  "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": {
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    {
      "status": "Ongoing",
      "city": "Exton",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "95190",
      "recalling_firm": "ProRx LLC",
      "address_1": "619 Jeffers Cir",
      "address_2": "",
      "postal_code": "19341-2540",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0652-2024",
      "product_description": "SEMAGLUTIDE 5mg/2mL (2.5mg/mL), Rx Only 2 mL Multiple Dose Vial, Rx Only, Compounded Drug, Mfd by: ProRX Exton, PA19341, NDC 84139-225-01",
      "product_quantity": "8,396 vials",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20240822",
      "center_classification_date": "20240905",
      "report_date": "20240911",
      "code_info": "Lot #: ProRx052424, BUD 11/23/2024 ProRx060724, BUD 12/06/2024 ProRx061124, BUD 12/10/2024 ProRx061924, BUD 12/18/2024",
      "more_code_info": ""
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}