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

MAUDE Adverse Event Report: CONAIR CORPORATION CONAIR SCALE BMI SCALE

  • 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
 

CONAIR CORPORATION CONAIR SCALE BMI SCALE Back to Search Results
Device Problem Burst Container or Vessel (1074)
Patient Problem Injury (2348)
Event Date 02/17/2016
Event Type  Injury  
Manufacturer Narrative
On (b)(6) 2016: - the consumer has discarded the device. Therefore, an evaluation will not be possible. Consumer has requested a replacement. A replacement will be sent to the consumer once photos of purchase has been received.
 
Event Description
On (b)(6) 2016 - consumer alleges the glass on the scale exploded when placed on the floor. The consumer received cuts on hands and feet. The scale was discarded. Consumer will submit photos as proof of purchase. The consumer has requested a replacement.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameCONAIR SCALE
Type of DeviceBMI SCALE
Manufacturer (Section D)
CONAIR CORPORATION
1 cummings point rd
stamford CT 06902
MDR Report Key5463925
MDR Text Key39158888
Report Number1222304-2016-00015
Device Sequence Number0
Product Code MNW
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation
Type of Report Initial
Report Date 02/17/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/26/2016
Is this an Adverse Event Report? Yes
Device Operator
Was Device Available for Evaluation? No
Is the Reporter a Health Professional?
Was the Report Sent to FDA?
Event Location No Information
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

Patient Treatment Data
Date Received: 02/26/2016 Patient Sequence Number: 1
-
-