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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BECTON DICKINSON AND CO. SYRINGE PISTON

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BECTON DICKINSON AND CO. SYRINGE PISTON Back to Search Results
Device Problem Device Markings/Labelling Problem (2911)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  No Answer Provided  
Event Description
Our pharmacy technicians have noticed that the print on bd syringes is fading/easily rubbing off causing syringe markings to be absent, and in some cases there are no markings at all on the syringe. In some cases, the syringe hasn't even been removed from the packaging. Severity: circumstances or events have capacity to cause error. (b)(6).
 
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Brand NameSYRINGE PISTON
Type of DeviceSYRINGE PISTON
Manufacturer (Section D)
BECTON DICKINSON AND CO.
MDR Report Key8208480
MDR Text Key132205099
Report NumberMW5082725
Device Sequence Number1
Product Code FMF
Combination Product (y/n)N
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 08/10/2018
1 Device was Involved in the Event
0 Patients were Involved in the Event:
Date FDA Received12/31/2018
Is this an Adverse Event Report? No
Is this a Product Problem Report? No
Device Operator
Was Device Available for Evaluation? No Answer Provided
Is the Reporter a Health Professional? No Answer provided
Was the Report Sent to FDA?
Event Location No Information
Was Device Evaluated by Manufacturer?
Is the Device Single Use?
Is This a Reprocessed and Reused Single-Use Device?
Type of Device Usage

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