{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Flower Mound",
      "address_1": "1410 Lakeside Pkwy Ste 100",
      "reason_for_recall": "The potential hazard that can arise for the combination of the missing screws and the overloading by the end user is insufficient mount force that causes the equipment to fall.",
      "address_2": "",
      "product_quantity": "292 devices (in US)",
      "code_info": "\"Serial Numbers:   100000000098399  100000000099187  100000000099193  100000000093937  100000000094391  100000000093936  100000000087555  100000000091032  100000000093938  100000000093928  100000000093939  100000000098397  100000000092672  100000000093927  100000000106675  100000000106685  100000000109560  100000000109569  100000000109570  100000000086360  100000000089194  100000000091766  100000000091778  100000000098401  100000000099325  100000000103228  100000000090520  100000000102434  100000000102439  100000000103111  100000000088303  100000000089467  100000000094993  100000000095927  100000000101580  100000000092699  100000000101590  100000000101591  100000000103686  100000000109291  100000000097048  100000000112633  100000000087549  100000000094982  100000000091762  100000000112607  100000000112609  100000000091531  100000000106681  100000000106682  100000000106684  100000000106159  100000000091728  100000000103271  100000000090522  100000000099356  100000000089970  100000000090530",
      "center_classification_date": "20170329",
      "distribution_pattern": "Worldwide distribution - United States Nationwide - Australia, Canada, Great Britain, Japan, Netherlands and Puerto Rico",
      "state": "TX",
      "product_description": "The Stryker Visum¿ LED Surgical Lighting system is intended to illuminate the operative site during surgical procedures with high intensity light. Affected part numbers are 0682001432 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P/FP), 0682001286 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P/FP), 0682001298 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P), 0682001299 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 5P/5P), 0682001300 (EDS LIGHT SUSPENSION, CENTRAL AXIS, FP/5P/5P), 0682001433 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P), 0682001434 (EDS LIGHT SUSPENSION, CENTRAL AXIS, 9P/5P), 0682001435 (EDS LIGHT SUSPENSION, CENTRAL AXIS, FP/9P/5P)    Product Usage:  The Stryker Visum LED Surgical Lighting system is intended to illuminate the operative site during surgical procedures with high intensity light",
      "report_date": "20170405",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Communications",
      "recall_number": "Z-1699-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "76633",
      "termination_date": "20180108",
      "more_code_info": "",
      "recall_initiation_date": "20170228",
      "postal_code": "75028-4026",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}