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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STAIR PRO - MODEL 6252; STRETCHER, HAND-CARRIED
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STAIR PRO - MODEL 6252; STRETCHER, HAND-CARRIED Back to Search Results
Catalog Number 6252000000
Device Problem Difficult or Delayed Positioning (1157)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 08/05/2021
Event Type  malfunction  
Event Description
It was reported the tracks on the stair chair were replaced, possibly indicating the chair was difficult to maneuver (no tip).No model number or serial number was provided at this time.There are no reports of patient involvement or adverse consequences.
 
Event Description
It was reported the tracks on the stair chair were replaced, possibly indicating the chair was difficult to maneuver (no tip).The serial number has not been provided.There are no reports of patient involvement or adverse consequences.
 
Manufacturer Narrative
The investigation is complete and the model number of the device has been provided.Product information in d tab as well as h codes have been updated to reflect investigation results.
 
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Brand Name
STAIR PRO - MODEL 6252
Type of Device
STRETCHER, HAND-CARRIED
MDR Report Key12314433
MDR Text Key266255737
Report Number0001831750-2021-01298
Device Sequence Number1
Product Code FPP
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type other
Type of Report Initial,Followup
Report Date 10/22/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator No Information
Device Catalogue Number6252000000
Was Device Available for Evaluation? Yes
Initial Date Manufacturer Received 08/05/2021
Initial Date FDA Received08/12/2021
Supplement Dates Manufacturer Received08/05/2021
Supplement Dates FDA Received10/22/2021
Was Device Evaluated by Manufacturer? No
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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