{
  "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": "2026-09-05",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "220096",
      "product_res_number": "Z-2282-2026",
      "event_date_initiated": "2026-05-06",
      "event_date_posted": "2026-06-01",
      "recall_status": "Open, Classified",
      "res_event_number": "98894",
      "product_code": "JCX",
      "k_numbers": [
        "K132671"
      ],
      "product_description": "Neptune Smart Docking Station (120V), Catalog Number 0770-100-000, part of the Neptune Waste Management System",
      "code_info": "GTIN 07613327634914, Serial Number 2521008873",
      "firm_fei_number": "3015967359",
      "recalling_firm": "Stryker Corporation",
      "address_1": "1941 Stryker Way",
      "city": "Portage",
      "state": "MI",
      "postal_code": "49002-9711",
      "additional_info_contact": "Brooke Thompson\n269-800-1941",
      "reason_for_recall": "It has been identified that the impacted docking station (SN 2521008873) was not product released from manufacturing and may not have completed required testing prior to being shipped to your facility. There is a potential risk of electrical shock due to the device s safety testing being unverifiable.",
      "root_cause_description": "Nonconforming Material/Component",
      "action": "Stryker issued an URGENT Medical Device Field Action notice to its consignee on 5/6/2026 via FedEx.  The notice explained the issue, potential risk and requested the consignee locate and quarantine the device.  The consignee was directed to contact their Stryker Sales Rep to help schedule replacement of the affected device.\nFor questions of concerns, contact Brooke Thompson at Instruments.Recalls@stryker.com.",
      "product_quantity": "1 unit",
      "distribution_pattern": "US Nationwide distribution in the state of Indiana.",
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        "device_name": "Apparatus, Suction, Ward Use, Portable, Ac-Powered",
        "medical_specialty_description": "General, Plastic Surgery",
        "regulation_number": "878.4780",
        "device_class": "2"
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}