FDA Adverse Event Malfunction Summary report: N

INTIMA-II 18GAX1.16IN PRN SLM

MDR report key: 8575457 · Received May 2, 2019

Report

Report Number
3006948883-2019-00333
Event Type
Malfunction
Date Received
May 2, 2019
Date of Event
April 15, 2019
Report Date
May 29, 2019
Manufacturer
BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.
Product Code
FOZ
PMA / PMN Number
N/A
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION: A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 8171128. OUR RECORDS SHOW THAT THIS IS THE ONLY INSTANCE OF THIS ISSUE OCCURRING IN THIS PRODUCTION BATCH. ACCORDING TO THE SAMPLING PLAN APPLIED FOR PRODUCT PERFORMANCE, THIS LOT WAS ACCEPTED AND RELEASED WITHOUT DEFECTS BEING NOTED DURING THE FINAL ASSEMBLY OR VISUAL INSPECTIONS. UNFORTUNATELY A SAMPLE COULD NOT BE OBTAINED FOR EVALUATION AND TESTING. WITHOUT THE ABILITY TO INVESTIGATE THE AFFECTED UNIT OUR QUALITY ENGINEERS WERE UNABLE TO DETERMINE THE ROOT CAUSE FOR THIS COMPLAINT.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE INTIMA-II 18GAX1.16IN PRN SLM EXPERIENCED PRODUCT DAMAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS FOUND THERE WAS A CRACK ON TH SIDE OF NEEDLE LEADING TO BLEED.

Additional Manufacturer Narrative · 1

A DEVICE EVALUATION IS ANTICIPATED, BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE INTIMA-II 18GAX1.16IN PRN SLM EXPERIENCED PRODUCT DAMAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: IT WAS FOUND THERE WAS A CRACK ON THE SIDE OF NEEDLE LEADING TO BLEED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
365281 INTIMA-II 18GAX1.16IN PRN SLM IV CATHETER FOZ BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD. 8171128

Patients

Seq Age Sex Outcome Treatment
1 Other