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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: FERNO-WASHINGTON, INC. INX FOR INLINE
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FERNO-WASHINGTON, INC. INX FOR INLINE Back to Search Results
Model Number 0015803
Device Problem Mechanical Jam (2983)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 02/08/2024
Event Type  malfunction  
Event Description
It was alleged after unloading a 600lb patient from the ambulance, the stretcher, while in the unloading position, would not respond to lower into the transport position.A device was used to remove the patient from the stretcher onto a hospital cot.No injuries were reported as a result.The stretcher was then lowered using the manual mode and the issue has not been able to be replicated since.The stretcher has been removed from service pending evaluation.
 
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Brand Name
INX FOR INLINE
Type of Device
INX FOR INLINE
Manufacturer (Section D)
FERNO-WASHINGTON, INC.
70 wiel way
wilmington OH 45177
Manufacturer (Section G)
FERNO-WASHINGTON, INC.
70 wiel way
wilmington OH 45177
Manufacturer Contact
dawn greene
70 wiel way
wilmington, OH 45177
9372832900
MDR Report Key18818695
MDR Text Key337640615
Report Number1523574-2024-00014
Device Sequence Number1
Product Code FPO
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 Health Care Professional
Type of Report Initial
Report Date 03/01/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/01/2024
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number0015803
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Date Manufacturer Received02/09/2024
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
Patient Weight272 KG
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