FDA Adverse Event Malfunction Summary report: N

SYR 10 ML FIL SALINE SHORTLENGTH PLUNGER ROD

MDR report key: 8918893 · Received August 21, 2019

Report

Report Number
1911916-2019-00846
Event Type
Malfunction
Date Received
August 21, 2019
Date of Event
July 18, 2019
Report Date
August 21, 2019
Manufacturer
BECTON DICKINSON AND COMPANY
Product Code
NGT
UDI-DI
30382903064992
PMA / PMN Number
K161552
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

INVESTIGATION SUMMARY: ONE SAMPLES WAS RECEIVED. IT HAS THE PLUNGER ROD- RUBBER STOPPER; IT HAS TIP CAP AND 5ML OF SOLUTION. THE PLUNGER ROD IS SEPARATED FROM THE RUBBER STOPPER. THE PLUNGER ROD WAS SCREWED BACK TO THE RUBBER STOPPER, THEN PULLED UP TEN TIMES AND STAYED ASSEMBLED. THE POSIFLUSH PRODUCT IS DESIGNED TO FLUSH THE IV LINES, ONE SINGLE USE, NOT TO DRAWING BLOOD. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. INFORMATION WILL BE CAPTURED ON TREND REPORTS AND MONITORED MONTHLY. OUR BUSINESS TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR IDENTIFICATION OF EMERGING TRENDS. A DEVICE HISTORY RECORD REVIEW WAS COMPLETED WITH ZERO DEFECTS FOUND. NO QUALITY NOTIFICATIONS WERE WRITTEN FOR THIS BATCH, NOR FOR THE ASSOCIATED ASSEMBLY BATCHES. INVESTIGATION CONCLUSION: THIS IS THE 2ND COMPLAINT FOR THE LOT# 9002663 FOR THE SAME DEFECT OR SYMPTOM. THERE WAS NO DOCUMENTATION OF ISSUES FOR THE COMPLAINT OF BATCH 9002663 DURING THE PRODUCTION RUN. ROOT CAUSE DESCRIPTION: ROOT CAUSE OFF LABEL USE. THE POSIFLUSH PRODUCT IS DESIGNED TO FLUSH THE IV LINES, ONE SINGLE USE, NOT TO DRAWING BLOOD.

Description of Event or Problem · 1

IT WAS REPORTED THAT PLUNGER SEPARATION OCCURRED DURING USE WITH A SYR 10 ML FIL SALINE SHORT LENGTH PLUNGER ROD. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER. "THE FLUSHES ARE NOT COMING APART UNLESS LABS ARE BEING DRAWN AND THE NURSES ARE PULLING BACK TO OBTAIN THE WASTE. THE HANDLE CAN BE SCREWED BACK INTO THE RUBBER PIECE, BUT THAT IS NOT BEST PRACTICE EITHER."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
712883 SYR 10 ML FIL SALINE SHORTLENGTH PLUNGER ROD INTERVASCULAR CATHETER NGT BECTON DICKINSON AND COMPANY 9002663 30382903064992

Patients

Seq Age Sex Outcome Treatment
1 10 YR Other