{
  "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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  "results": [
    {
      "cfres_id": "85062",
      "product_res_number": "Z-0148-2010",
      "event_date_initiated": "2009-09-02",
      "event_date_posted": "2009-11-09",
      "recall_status": "Terminated",
      "event_date_terminated": "2011-02-16",
      "res_event_number": "53251",
      "product_code": "FPP",
      "product_description": "Stryker Medical Stair-PRO Stair Chair with wheels, patient transport device, Model 6251.",
      "code_info": "Serial numbers 080639995, 080640003, 081039395, 080639996, 080640004, 081039396, 080639997, 080739856, 081039397, 080639998, 080739857, 081039398, 080639999, 080739858, 081039399, 080640000, 080739859, 081039400, 080640001, 080739860, 081039401,   080640002, 080740001, 081039402, 080439860, 080439861, 080439862, 080439863, 080439864, 080439865, 080439866, 080439867, 080441124, 080439868, 080541216, 080541293, 080541294, 080541295, 080541296, 080541297, 080541298, 081039403,  081039404, 081040900, 081040901, 081040902, 090139365, 090139366, 090139367, 090139368, 090139369, 090139373, 090140687, 090140691, 090140692, 090140693, 090140694, 090140688, 090140695, 090140689, 090140696, 090140690, 090241071, 090241072 and 090241073.",
      "firm_fei_number": "1831750",
      "recalling_firm": "Stryker Medical Div. of Stryker Corporation",
      "address_1": "3800 East Centre Ave.",
      "city": "Portage",
      "state": "MI",
      "postal_code": "49002",
      "additional_info_contact": "269-324-6609",
      "reason_for_recall": "The front of the handle may become detached from the chair, which could result in a patient fall or an operator injury.",
      "root_cause_description": "Device Design",
      "action": "Consignees were sent a letter titled URGENT MEDICAL DEVICE CORRECTION dated 9/9/09, advising them of the problem and to remove the devices from service until they have been repaired.   U.S. customers were notified that Stryker will complete the correction while international customers were sent a kit with instructions for completion of the correction.  International consignees were told that Stryker will complete the correction if the consignee does not feel comfortable in doing so. Questions or comments regarding this issue should be addressed to Sarah Marie Puterbaugh of Stryker Medical at (800) 869-0770 ext. 6902.",
      "product_quantity": "65",
      "distribution_pattern": "Worldwide distribution - Colorado, Ohio, Wisconsin, and Germany, Italy, Netherlands, Poland and Switzerland.",
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