{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Fremont",
      "address_1": "47900 Bayside Pkwy",
      "reason_for_recall": "Stryker Neurovascular has become aware that some 3-Pack Stroke Fast Packs and Trevo Procedure Packs  were manufactured using a carton sleeve where the sleeve label contents did not match the physical contents within the pack.",
      "address_2": "",
      "product_quantity": "1 unit",
      "code_info": "Lot Number QX10100894. Exp. Date 28-Oct-18",
      "center_classification_date": "20171221",
      "distribution_pattern": "International Distribution to: Germany, Slovakia and Israel.",
      "state": "CA",
      "product_description": "Trevo(TM) XP ProVue Procedure Pack, TREVO(TM) XP PROVUE RETRIEVER, 6 mm, 25 mm, .Excelsior(TM) XT-27(TM) 1 TIP STRAIGHT, 150 cm, 6 cm, Microcatheter; UPN 93068    Stroke intervention kit",
      "report_date": "20171227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Neurovascular",
      "recall_number": "Z-0277-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "78607",
      "termination_date": "20191104",
      "more_code_info": "",
      "recall_initiation_date": "20171103",
      "postal_code": "94538-6515",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}