{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "77161",
      "product_res_number": "Z-0841-2012",
      "event_date_initiated": "2008-11-12",
      "event_date_posted": "2012-01-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-01-26",
      "res_event_number": "50776",
      "product_code": "HCG",
      "k_numbers": [
        "K060747"
      ],
      "product_description": "Axium Detachable Coil System Model Number: QC-2-2-3D.\n\nThe AXIUM DETACHABLE COIL SYSTEM consists of a platinum embolization coil attached to a composite implant delivery pusher with a radiopaque positioning marker and a hand-held I.D. (instant detacher) which when activated detached the coil from the delivery pusher tip. Some of the AX IUM Detachable coils are enlaced with PGLA microfilaments or Nylon microfilaments. I.D. (instant detached) is sold separately.",
      "code_info": "Lot Number: 5871057",
      "firm_fei_number": "3004904811",
      "recalling_firm": "Micro Therapeutics Inc, dba ev3 Neurovascular",
      "address_1": "9775 Toledo Way",
      "city": "Irvine",
      "state": "CA",
      "postal_code": "92618-1811",
      "additional_info_contact": "949-839-3700",
      "reason_for_recall": "ev3 Neurovascular has identified an incorrect expiration date on the label of one lot of ev3 Axium coils Catalog QC-2-2-3D.  This lot 5871057 shows an expiration date of 0211-04.  The expiration date should read 2011-04.  There are no functional issues with the coils in question as the appropriate expiration date is 2011.",
      "root_cause_description": "Process control",
      "action": "ev3 Neurovascular sent a \"NOTIFICATION OF RECALL\" letter dated November 6, 2008 to all affected customers.  The letter identifies the product, problem, and the actions to be taken by the customers.  The letter instructs customers to stop use and segregate the affected product from inventory.  A reply form was attached to the letter for customers to complete and fax to Customer Service at (763)398-7001.  Customer Service will issue an RGA number for the return of the affected product.  Contact the Quality Systems Manager at (949) 680-1305 for questions regarding this notice.",
      "product_quantity": "16",
      "distribution_pattern": "Worldwide Distribution-USA (nationwide) including the states of  CA, CT, NE, NV, and WI. and the countries of Argentina, Brazil, Colombia, and Egypt.",
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        "device_name": "Device, Neurovascular Embolization",
        "medical_specialty_description": "Neurology",
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