• 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 BIA SCALES

  • 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 BIA SCALES Back to Search Results
Model Number WW711
Device Problem Break (1069)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 11/04/2018
Event Type  malfunction  
Manufacturer Narrative
On 12/3/2018 - the consumer discarded the product and agreed to a replacement. An investigation will not be performed do to the product being discarded.
 
Event Description
On (b)(6) 2018 - the consumer claims that glass on the unit shattered. No injuries occurred and the consumer agree to a replacement. The consumer discarded the product, therefore an investigation will not be completed.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand NameCONAIR
Type of DeviceBIA SCALES
Manufacturer (Section D)
CONAIR CORPORATION
1 cummings point rd
stamford 06902
Manufacturer Contact
1 cummings point rd.
stamford, 
MDR Report Key8126025
MDR Text Key129333829
Report Number1222304-2018-00027
Device Sequence Number1
Product Code MNW
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation
Type of Report Initial
Report Date 11/05/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/03/2018
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator
Device Model NumberWW711
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: 12/03/2018 Patient Sequence Number: 1
-
-