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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BD SHARPS CONTAINER (BD)1.5 QT; CONTAINER, SHARPS
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BD SHARPS CONTAINER (BD)1.5 QT; CONTAINER, SHARPS Back to Search Results
Device Problem Defective Component (2292)
Patient Problem Insufficient Information (4580)
Event Type  malfunction  
Event Description
Spontaneous, patient advised that the sharps container that she received is defective; unknown if device available for return; unknown lot /expiration.No further information known.Reported to (b)(6) by: patient/caregiver.
 
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Brand Name
SHARPS CONTAINER (BD)1.5 QT
Type of Device
CONTAINER, SHARPS
Manufacturer (Section D)
BD
MDR Report Key10919279
MDR Text Key218986109
Report NumberMW5098139
Device Sequence Number1
Product Code MMK
Combination Product (y/n)Y
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 11/11/2020
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/27/2020
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator No Information
Is the Reporter a Health Professional? Yes
Patient Sequence Number1
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