{
  "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": {
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  "results": [
    {
      "cfres_id": "160218",
      "product_res_number": "Z-0347-2018",
      "event_date_initiated": "2017-11-28",
      "event_date_created": "2018-01-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2020-04-28",
      "res_event_number": "78716",
      "product_code": "NRY",
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      "code_info": "UPN/Model No. 80052; Lot 63034",
      "firm_fei_number": "3008853977",
      "recalling_firm": "Stryker Neurovascular",
      "address_1": "47900 Bayside Pkwy",
      "city": "Fremont",
      "state": "CA",
      "postal_code": "94538-6515",
      "reason_for_recall": "Stryker Neurovascular has become aware that at least 1 (one) Trevo XP Provue System was manufactured where the carton sleeve did not match the physical contents of the pack.",
      "root_cause_description": "Packaging process control",
      "action": "The affected consignees will be notified via letter sent a courier beginning 11/28/17. A response form has been provided which customers have been asked to complete, and correct affected product is being requested.",
      "distribution_pattern": "OUS only - NL, FR, IT, DE, BE",
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        "medical_specialty_description": "Cardiovascular",
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        "device_class": "2"
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    }
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}