{
  "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": "2026-08-13",
    "results": {
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      "recall_status": "Terminated",
      "event_date_terminated": "2006-10-10",
      "res_event_number": "32667",
      "product_code": "GWG",
      "product_description": "Remington Medical, Inc., 8 French-Sheath Only, Size 8 French, Single Use. Ethylene Oxide sterilized.",
      "code_info": "Lot No. 041603, 041731, 050201, 050274",
      "firm_fei_number": "1000132370",
      "recalling_firm": "Remington Medical Inc.",
      "address_1": "6830 Meadowridge Ct",
      "city": "Alpharetta",
      "state": "GA",
      "postal_code": "30005-2202",
      "additional_info_contact": "Maria Granito\n800-989-0057",
      "reason_for_recall": "The Tear-Away introducer sheath in the Disposable Tear-Away Vascular Introducer kits may exhibit cracked hubs/handles and/or improper peeling of the sheath during use.",
      "root_cause_description": "Other",
      "action": "A recall letter was sent to each consignee July 6th through July 11, 2005 requesting that they examine any product on hand.  The letter also indicated that a representative would be contacting them in follow-up to the letter.",
      "product_quantity": "1500 units",
      "distribution_pattern": "AL, AR, CA, CO, FL, GA, IN, IA, MD, MN, MO, NE, NV, NY, OH, OK, OR, PA, RI, TX, UT, VA, WA, WI",
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