{
  "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": "2026-08-13",
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      "cfres_id": "30589",
      "product_res_number": "Z-0267-04",
      "event_date_initiated": "2003-12-01",
      "event_date_posted": "2003-12-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-04-12",
      "res_event_number": "27824",
      "product_code": "INK",
      "product_description": "Stryker brand Model 1550 Synergy Extended Stay Stretcher",
      "code_info": "All stretchers manufactured between 1/1/1993 and 11/07/2003.",
      "firm_fei_number": "1831750",
      "recalling_firm": "Stryker Medical",
      "address_1": "6300 Sprinkle Rd",
      "city": "Kalamazoo",
      "state": "MI",
      "postal_code": "49001",
      "additional_info_contact": "Renata Sila\n800-669-4968 Ext. 6689",
      "reason_for_recall": "The user may be pinched by the siderail when raising or lowering the siderail.",
      "root_cause_description": "Other",
      "action": "Recall letters dated 12/1/03 were sent to each consignee notifying them that Stryker would be contacting them to modify the siderail assembly.",
      "product_quantity": "3903",
      "distribution_pattern": "United States, Canada, Hong Kong, Israel, Mexico and Syria.",
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        "medical_specialty_description": "Physical Medicine",
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}