{
  "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": "2026-08-27",
    "results": {
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  "results": [
    {
      "cfres_id": "66908",
      "product_res_number": "Z-0577-2008",
      "event_date_initiated": "2007-11-23",
      "event_date_posted": "2008-02-26",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-05-01",
      "res_event_number": "46158",
      "product_code": "JEB",
      "product_description": "TENET Medical Engineering Wrist Stabilization Kit, Small; REF (Part) #7691; Sterile; manufactured by TENET Medical Engineering, Calgary, Alberta, Canada  T2Z 4M3.",
      "code_info": "Lot Number: 20060605.",
      "firm_fei_number": "3004750931",
      "recalling_firm": "Tenet Medical Engineering Inc",
      "address_1": "11979 40th St Se /#203 Ab",
      "city": "Calgary",
      "country": "Canada",
      "reason_for_recall": "Sterility compromised:  Sterility seals on some of the firm's wrist stabilization kit pouches may be compromised.",
      "root_cause_description": "Packaging process control",
      "action": "TENET notified US distributor consignee via Urgent Product Recall Notification letter sent FedEx on 11/23/07.  Consignee asked to return product and to contact their consignees to also return product.",
      "product_quantity": "300 units.",
      "distribution_pattern": "Nationwide Distribution.",
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        "device_name": "Table, Surgical With Orthopedic Accessories, Manual",
        "medical_specialty_description": "General, Plastic Surgery",
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