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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO STAIR PRO - MODEL 6252; STRETCHER, HAND-CARRIED
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STRYKER MEDICAL-KALAMAZOO STAIR PRO - MODEL 6252; STRETCHER, HAND-CARRIED Back to Search Results
Catalog Number 6252000000
Device Problems Bent (1059); Break (1069)
Patient Problems Abrasion (1689); Injury (2348)
Event Date 07/09/2015
Event Type  Injury  
Event Description
It was reported that a staff member was moving the patient while it was wet outside and the staff member slipped dropping the chair with the patient.This caused 1 handle of the chair to break and the 2nd handle to bend.The patient received an abrasion to their arm.The staff member hurt their wrist.
 
Manufacturer Narrative
The device has not been repaired at this time.
 
Manufacturer Narrative
It was reported that there was patient involvement in which the patient received an abrasion on their arm which could not be confirmed due to them refusing treatment.The nurse also received a very minor strain in which she was put on light duty for one day.
 
Event Description
It was reported that a staff member was moving the patient while it was wet outside and the staff member slipped dropping the chair with the patient.
 
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Brand Name
STAIR PRO - MODEL 6252
Type of Device
STRETCHER, HAND-CARRIED
Manufacturer (Section D)
STRYKER MEDICAL-KALAMAZOO
3800 east centre avenue
portage MI 49002
Manufacturer (Section G)
STRYKER MEDICAL-KALAMAZOO
3800 east centre avenue
portage MI 49002
Manufacturer Contact
brian thompson
3800 east centre avenue
portage, MI 49002
2693292100
MDR Report Key4972974
MDR Text Key21767855
Report Number0001831750-2015-00383
Device Sequence Number1
Product Code FPP
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type User Facility,user facility
Reporter Occupation Other
Type of Report Initial
Report Date 07/09/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
Device Catalogue Number6252000000
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 07/09/2015
Initial Date FDA Received08/05/2015
Was Device Evaluated by Manufacturer? Yes
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
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