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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HILL-ROM, INC. STRETCHER; STRETCHER, WHEELED

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HILL-ROM, INC. STRETCHER; STRETCHER, WHEELED Back to Search Results
Device Problems Mechanical Problem (1384); Activation Failure (3270); Fail-Safe Did Not Operate (4046)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
(b)(6) was notified of a potentially reportable complaint involving a product for which (b)(6) is not the original equipment manufacturer of the reported device.The customer alleged a manufacturer hill-rom stretcher, serial number (b)(6) that had head end brakes that would not engage.Please find additional contact information below.This report reflects information received by fda in the form of a notification per 803.22 (b)(2).
 
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Brand Name
STRETCHER
Type of Device
STRETCHER, WHEELED
Manufacturer (Section D)
HILL-ROM, INC.
MDR Report Key17316558
MDR Text Key319075027
Report NumberMW5119351
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 Voluntary
Reporter Occupation Unknown
Type of Report Initial
Report Date 06/29/2023
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
Initial Date Manufacturer Received Not provided
Initial Date FDA Received07/12/2023
Patient Sequence Number1
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