{
  "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": "43292",
      "product_res_number": "Z-0589-06",
      "event_date_initiated": "2005-12-14",
      "event_date_posted": "2006-03-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-03-22",
      "res_event_number": "34219",
      "product_code": "MIH",
      "pma_numbers": [
        "P040002"
      ],
      "product_description": "Powerlink System for Abdominal Aortic Aneurysm (Endoluminal Bifurcated Prosthesis with Delivery System) Model No. 25-16-140BL",
      "code_info": "Lot # W05-0884",
      "firm_fei_number": "1000125107",
      "recalling_firm": "Endologix Inc",
      "address_1": "13900 Alton Pkwy Ste 122 13900 Alton Pkwy",
      "address_2": "Ste 122",
      "city": "Irvine",
      "state": "CA",
      "postal_code": "92618-1621",
      "additional_info_contact": "Janet Fauls\n949-595-7203",
      "reason_for_recall": "The tip may separate from the catheter sheath inner core during insertion of the graft.  The delivery catheter is being recalled.  The implanted devices are not affected.",
      "root_cause_description": "Other",
      "action": "The three affected hospitals were contacted telephone and in writing (Recall Letters) sent via FedEx Endologix field personnel are scheduled to remove the product units by 12/16/05. \nNotices for Phase II of recall to 8 additional consignees for 6 additional models (9 lots) being recalled mailed 12/19-12/22/05.",
      "product_quantity": "9 (8 already used and 1 currently in distribution)",
      "distribution_pattern": "For units still in distribution: AZ, DE, KS, PA, & TN",
      "openfda": {
        "pma_number": [
          "P040043",
          "P210032",
          "P070027",
          "P100040",
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          "P990020",
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          "P990017",
          "P200030",
          "P020018",
          "P070016",
          "P200045",
          "P110032",
          "P070007"
        ],
        "device_name": "System, Endovascular Graft, Aortic Aneurysm Treatment",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3",
        "registration_number": [
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