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

MAUDE Adverse Event Report: CARROLL HEALTHCARE AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS; 880.5100

  • 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
 

CARROLL HEALTHCARE AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS; 880.5100 Back to Search Results
Model Number IHECHOHC
Device Problem Sticking (1597)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Event Description
Per provider, one rail not flipping back.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
AC-POWERED ADJUSTABLE HOSPITAL BED, INCLUDING RAILS
Type of Device
880.5100
Manufacturer (Section D)
CARROLL HEALTHCARE
994 hargrieve rd
london, ontario N6E 1P5
CA  N6E 1P5
Manufacturer (Section G)
CARROLL HEALTHCARE
994 hargrieve rd
london, ontario N6E 1P5
CA   N6E 1P5
Manufacturer Contact
gregory stevens
one invacare way
elyria, OH 44035
8003336900
MDR Report Key3827210
MDR Text Key4497576
Report Number3003433498-2014-00100
Device Sequence Number1
Product Code FNL
Combination Product (y/n)N
Reporter Country CodeCA
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Distributor
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 04/09/2014
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 Lay User/Patient
Device Model NumberIHECHOHC
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 04/09/2014
Initial Date FDA Received05/22/2014
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
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 Outcome(s) Other;
-
-