• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HILL-ROM TOTALCARE; BED, AC-POWERED ADJUSTABLE HOSPITAL

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

HILL-ROM TOTALCARE; BED, AC-POWERED ADJUSTABLE HOSPITAL Back to Search Results
Model Number 60035
Device Problems Positioning Problem (3009); Power Problem (3010)
Patient Problem Insufficient Information (4580)
Event Type  malfunction  
Event Description
On june 9, 2011, stryker medical was notified of a potentially reportable complaint involving a product for which stryker is not the manufacturer.The customer reported a hill-rom bed, serial number (b)(6); model 60035 total care had no power to the bed and the head of the bed goes down by itself.Please find additional contact information below.This report reflects information received by fda in the form of a notification per 803.22 (b)(2).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
TOTALCARE
Type of Device
BED, AC-POWERED ADJUSTABLE HOSPITAL
Manufacturer (Section D)
HILL-ROM
MDR Report Key17534442
MDR Text Key321459239
Report NumberMW5141343
Device Sequence Number1
Product Code FNL
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other
Type of Report Initial
Report Date 07/05/2011
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/12/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Model Number60035
Patient Sequence Number1
-
-