{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "47264",
      "product_res_number": "Z-0044-2007",
      "event_date_initiated": "2006-04-24",
      "event_date_posted": "2006-10-19",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-10-26",
      "res_event_number": "35960",
      "product_code": "NGT",
      "product_description": "0.9% Sodium Chloride Flush Syringe, 2.5 mL.   Product Code: E0100-30.  Manufactured by Excelsior Medical and distributed by Hospira, Lake Forest, IL under Hospira''s label, Syrex.",
      "code_info": "Product E0100-30, Lot 22-010-9D",
      "firm_fei_number": "1000122362",
      "recalling_firm": "Excelsior Medical Corp",
      "address_1": "1923 Heck Ave",
      "city": "Neptune",
      "state": "NJ",
      "postal_code": "07753-4428",
      "additional_info_contact": "Himanshu Naik\n732-643-6080",
      "reason_for_recall": "The syringe manufacturer mixed a pre-printed heparin labeled flush syringe with the saline syringes.",
      "root_cause_description": "Other",
      "action": "Excelsior notified Hospira of the recall on 4/24/2006.  Hospira notified Morris Dickson and Cardinal Health on 4/28/2006.",
      "product_quantity": "466,000 units",
      "distribution_pattern": "Worldwide.",
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        "device_name": "Saline, Vascular Access Flush",
        "medical_specialty_description": "General Hospital",
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}