{
  "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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      "cfres_id": "124913",
      "product_res_number": "Z-0903-2014",
      "event_date_initiated": "2013-12-30",
      "event_date_posted": "2014-01-31",
      "recall_status": "Terminated",
      "event_date_terminated": "2016-01-12",
      "res_event_number": "67191",
      "product_code": "JCX",
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      "product_description": "Neptune 2 Rover Ultra Waste Management System",
      "code_info": "Manufacturer Part Number 0702-002-000 (230V) All serial numbers",
      "firm_fei_number": "1811755",
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "address_1": "4100 E Milham Ave",
      "city": "Portage",
      "state": "MI",
      "postal_code": "49002-9704",
      "additional_info_contact": "269-323-7700",
      "reason_for_recall": "The purpose of this correction is to upgrade the Neptune 2 Waste Management Systems in the field to the recently obtained 510(k) clearance specifications.",
      "root_cause_description": "Device Design",
      "action": "On 12/30/13, Stryker sent an URGENT MEDICAL DEVICE UPDATE notification to consignees including government accounts and Sales Representatives, Stryker Canada and 3 in-house accounts and 1 account for lost rovers.  Domestic and government consignees were sent the notification by mail FedEx overnight, and Sales Representatives and Stryker Canada were sent the notification by email.  Notification described the affected product, instructions for the consignees, and upgrade information.  Stryker also stated that a training kit and in-servicing will be provided to consignees.  For questions regarding this recall, please contact Stryker Instruments: Monday-Friday 8am-5pm (EST)\r\nNeptune Customer Care Center 855-458-7441 or 269-389-2316\r\nstrykerinstrumentsrecalls@stryker.com",
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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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