{
  "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": "2026-07-07",
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    {
      "manufacturer_contact_zip_ext": "",
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      "report_to_fda": "*",
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      "pma_pmn_number": "",
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      "manufacturer_contact_plocal": "",
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      "manufacturer_g1_state": "",
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      "date_added": "20200427",
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          "implant_flag": "",
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          "brand_name": "STAIR PRO - MODEL 6252",
          "generic_name": "STRETCHER, HAND-CARRIED",
          "manufacturer_d_name": "STRYKER MEDICAL-KALAMAZOO",
          "manufacturer_d_address_1": "3800 EAST CENTRE AVENUE",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "PORTAGE",
          "manufacturer_d_state": "MI",
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          "manufacturer_d_country": "US",
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          "device_operator": "I",
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          "device_age_text": "DA",
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          "combination_product_flag": "N",
          "udi_di": "",
          "udi_public": "",
          "openfda": {
            "device_name": "Stretcher, Hand-Carried",
            "medical_specialty_description": "General Hospital",
            "regulation_number": "880.6900",
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        }
      ],
      "product_problems": [
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        "Protective Measures Problem"
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      "reporter_state_code": "MI",
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      "suppl_dates_mfr_received": "04/01/2020",
      "mfr_report_type": "",
      "manufacturer_contact_country": "",
      "date_changed": "20250803",
      "health_professional": "",
      "summary_report_flag": "Y",
      "manufacturer_g1_zip_code_ext": "",
      "manufacturer_contact_extension": "",
      "manufacturer_city": "",
      "manufacturer_contact_phone_number": "",
      "patient": [
        {
          "patient_sequence_number": "1",
          "date_received": "20200427",
          "sequence_number_treatment": [
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          "sequence_number_outcome": [
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          "patient_age": "",
          "patient_sex": "",
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          "patient_race": "",
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        }
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      "date_report": "20200428",
      "initial_report_to_fda": "",
      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "manufacturer_contact_city": "",
      "mdr_report_key": "10000296",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_manufacturer_received": "20200401",
      "manufacturer_name": "",
      "report_source_code": "Manufacturer report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
      "manufacturer_zip_code_ext": "",
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      "adverse_event_flag": "N",
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      "manufacturer_state": "",
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      "manufacturer_postal_code": "",
      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "189193354",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "1",
          "text": "THIS MDR IS A CONSOLIDATION OF RECORDS SUMMARIZED AS PART OF THE FDA VOLUNTARY MALFUNCTION SUMMARY REPORTING PROGRAM. 5 DEVICES WERE EVALUATED IN THE FIELD AND THE ISSUE WAS CONFIRMED; 4 DEVICES HAD MISSING COMPONENTS AND 1 DEVICE HAD BROKEN/DAMAGED COMPONENTS. THE DEVICES WERE REPAIRED AND RETURNED. 1 DEVICE IS PENDING EVALUATION. THERE WAS NO REMEDIAL ACTION TAKEN. THIS DEVICE IS NOT LABELED FOR SINGLE USE."
        },
        {
          "mdr_text_key": "189193355",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "THIS REPORT SUMMARIZES <NOE> 6 </NOE> MALFUNCTION EVENTS, WHERE IT WAS REPORTED THE DEVICE HAD MISSING OR DAMAGED RESTRAINTS. THERE WAS NO PATIENT INVOLVEMENT."
        },
        {
          "mdr_text_key": "318116980",
          "text_type_code": "Additional Manufacturer Narrative",
          "patient_sequence_number": "0",
          "text": "IT WAS ORIGINALLY REPORTED THAT 6 DEVICES EXPERIENCED THE REPORTED MALFUNCTION; HOWEVER, IT WAS DETERMINED THAT ONLY 1 DEVICE EXPERIENCED THIS MALFUNCTION; THE DEVICE HAD MISSING COMPONENTS. HAS BEEN UPDATED TO REFLECT THE CORRECTED INFORMATION."
        },
        {
          "mdr_text_key": "318116981",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "0",
          "text": "THIS REPORT SUMMARIZES <NOE> 1 </NOE> MALFUNCTION EVENT, WHERE IT WAS REPORTED THE DEVICE HAD MISSING OR DAMAGED RESTRAINTS.  THERE WAS NO PATIENT INVOLVEMENT."
        }
      ],
      "number_patients_in_event": "",
      "distributor_name": "",
      "manufacturer_g1_address_1": "",
      "distributor_zip_code": "",
      "manufacturer_contact_postal_code": "",
      "manufacturer_contact_exchange": "",
      "manufacturer_contact_pcountry": "",
      "suppl_dates_fda_received": "04/28/2020"
    }
  ]
}