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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONAIR CORPORATION CONAIR MASSAGER

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CONAIR CORPORATION CONAIR MASSAGER Back to Search Results
Model Number NM8
Device Problem Sparking (2595)
Patient Problem Insufficient Information (4580)
Event Date 10/14/2021
Event Type  malfunction  
Event Description
10/19/2021 - the consumer claims the device was sparking in the area by the cord. The consumer has accepted a replacement device.
 
Manufacturer Narrative
11/10/2021 - the consumer accepted a replacement product. Therefore the product will not be submitted to the manufacturer for an investigation.
 
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Brand NameCONAIR
Type of DeviceMASSAGER
Manufacturer (Section D)
CONAIR CORPORATION
1 cummings point rd.
stamford CT 06902
Manufacturer Contact
1 cummings point rd.
stamford, CT 06902
MDR Report Key12786032
MDR Text Key282225116
Report Number1222304-2021-00030
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 11/10/2021
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received11/10/2021
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model NumberNM8
Was Device Available for Evaluation? No Answer Provided
Was Device Evaluated by Manufacturer? No
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No

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