{
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    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-01",
    "results": {
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    {
      "status": "Ongoing",
      "city": "Exton",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "97808",
      "recalling_firm": "ProRx LLC",
      "address_1": "619 Jeffers Cir",
      "address_2": "N/A",
      "postal_code": "19341-2540",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "TX and UT",
      "recall_number": "D-0115-2026",
      "product_description": "Semaglutide Injection, 10 mg/4 mL (2.5 mg/mL), 4mL Multidose Vial, For Subcutaneous Use, Rx Only, Mfd by: ProRx, 619 Jeffers Cir, Exton, PA 19341.  NDC:  84139-225-04",
      "product_quantity": "8,400 vials",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20251015",
      "center_classification_date": "20251027",
      "report_date": "20251105",
      "code_info": "Lot, Best Use Date (BUD):  Lot PRORX050925-1, BUD November 4, 2025;  Lot ProRx051425-5, BUD November 10, 2025; Lot ProRx051425-6, BUD November 10, 2025"
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