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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: EMERSON METER; EMERSON METER

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EMERSON METER; EMERSON METER Back to Search Results
Device Problem Device Inoperable (1663)
Patient Problem Pain (1994)
Event Type  Other  
Event Description
Patient reported that her current meter doesn't work anymore she has to go deeper and deeper and when she pulls it out it really hurts.
 
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Brand Name
EMERSON METER
Type of Device
EMERSON METER
MDR Report Key5486249
MDR Text Key39940253
Report NumberMW5060787
Device Sequence Number1
Product Code CBK
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 03/03/2016
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/03/2016
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator No Information
Type of Device Usage N
Patient Sequence Number1
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