{
  "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": "2 units",
      "code_info": "Lot Number QPC30200039, Exp. Date 28-Aug-18; QPC30200114, Exp. Date 28-Mar18",
      "center_classification_date": "20171221",
      "distribution_pattern": "International Distribution to: Germany, Slovakia and Israel.",
      "state": "CA",
      "product_description": "Stroke Fast Pack(TM), Trevo(TM) XP, TREVO(TM) XP PROVUE RETRIEVER, 4 mm, 20 mm, ; Trevo(TM) Pro 18, TREVO PRO 18 MICROCATHETER, 0.021 in ID, 150 cm; AXS Catalyst(TM) 6,  Distal Access Catheter, 0.060 in, 132 cm; UPN M0033PK42022002    Stroke intervention kit",
      "report_date": "20171227",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Neurovascular",
      "recall_number": "Z-0276-2018",
      "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"
    }
  ]
}