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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: EQUASHIELD FEMALE LEUR LOCK CONNECTOR

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EQUASHIELD FEMALE LEUR LOCK CONNECTOR Back to Search Results
Lot Number 13-21281
Device Problems Leak/Splash (1354); Chemical Spillage (2894)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 03/05/2014
Event Type  No Answer Provided  
Event Description
Twenty ml of docetaxel (chemo) leaked out from the connection between the infusion set and female luer lock closed system transfer device.Reason for use: to infuse docetaxel.Infuse docetaxel to patient.
 
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Brand Name
FEMALE LEUR LOCK CONNECTOR
Type of Device
LEUR LOCK
Manufacturer (Section D)
EQUASHIELD
MDR Report Key3675346
MDR Text Key4301515
Report NumberMW5034887
Device Sequence Number2
Product Code FPA
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Pharmacist
Type of Report Initial
Report Date 03/06/2014
2 Devices were Involved in the Event: 1   2  
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Lot Number13-21281
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received03/07/2014
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age62 YR
Patient Weight64
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