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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONAIR CORPORATION CONAIR CORPORATION BMI SCALE

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CONAIR CORPORATION CONAIR CORPORATION BMI SCALE Back to Search Results
Model Number WW711XF
Device Problem Explosion (4006)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 07/03/2020
Event Type  malfunction  
Manufacturer Narrative
07/16/2020:the consumer accepted a product replacement. Therefore, the consumer will not be returned the product to the manufacturer for an investigation.
 
Event Description
7/6/2020: the consumer claims the product exploded. The consumer accepted a replacement.
 
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Brand NameCONAIR CORPORATION
Type of DeviceBMI SCALE
Manufacturer (Section D)
CONAIR CORPORATION
1 cummings point rd.
stamford,
Manufacturer Contact
1 cummings point rd.
stamford, 
MDR Report Key10388145
MDR Text Key203299251
Report Number1222304-2020-00008
Device Sequence Number1
Product Code MNW
Combination Product (y/n)N
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 07/06/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/10/2020
Is this an Adverse Event Report? Yes
Device Operator
Device Model NumberWW711XF
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: 08/10/2020 Patient Sequence Number: 1
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