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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO POWER PRO AMBULANCE COT - OBS; STRETCHER, WHEELED
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STRYKER MEDICAL-KALAMAZOO POWER PRO AMBULANCE COT - OBS; STRETCHER, WHEELED Back to Search Results
Catalog Number 6500000000
Device Problem Adverse Event Without Identified Device or Use Problem (2993)
Patient Problem Physical Entrapment (2327)
Event Date 02/19/2019
Event Type  Injury  
Event Description
It was reported that allegedly the emt got his finger caught and pinched between the legs of the cot.This allegedly required the emt to go to the emergency room.No patients were involved or harmed.
 
Manufacturer Narrative
The customer reported that they do not need anyone reaching out from quality and are not requiring any further investigation.
 
Event Description
It was reported that allegedly the emt got his finger caught and pinched between the legs of the cot.This allegedly required the emt to go to the emergency room.No patients were involved or harmed.
 
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Brand Name
POWER PRO AMBULANCE COT - OBS
Type of Device
STRETCHER, WHEELED
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 Key8438340
MDR Text Key139407433
Report Number0001831750-2019-00284
Device Sequence Number0
Product Code FPO
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type user facility
Reporter Occupation Other
Type of Report Initial,Followup
Report Date 03/27/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/20/2019
Is this an Adverse Event Report? Yes
Device Operator No Information
Device Catalogue Number6500000000
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received02/20/2019
Was Device Evaluated by Manufacturer? Yes
Date Device Manufactured02/15/2006
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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