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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO UNKNOWN_MEDICAL_PRODUCT; STRETCHER, HAND-CARRIED
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STRYKER MEDICAL-KALAMAZOO UNKNOWN_MEDICAL_PRODUCT; STRETCHER, HAND-CARRIED Back to Search Results
Catalog Number UNK_MED
Device Problem Break (1069)
Patient Problems Fall (1848); Injury (2348)
Event Date 02/18/2013
Event Type  Injury  
Event Description
It was reported that the patient was strapped to a stair chair and being transported when the handle on the chair broke causing the patient to be dropped and an emt fell on top of the patient.It was reported that the patient was injured during the event however details were not provided.
 
Manufacturer Narrative
The catalog number of the device has been updated to unknown due to the device not being available for evaluation.
 
Event Description
It was reported that the patient was strapped to a stair chair and being transported when the handle on the chair broke causing the patient to be dropped and an emt fell on top of the patient.It was reported that the patient was injured during the event however details were not provided.
 
Manufacturer Narrative
Device not returned.
 
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Brand Name
UNKNOWN_MEDICAL_PRODUCT
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 Key4529994
MDR Text Key5814744
Report Number0001831750-2015-00072
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 Other
Reporter Occupation Other
Type of Report Initial,Followup
Report Date 01/30/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/20/2015
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Other
Device Catalogue NumberUNK_MED
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received01/30/2015
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
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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