FDA Adverse Event Malfunction Summary report: N

BD LUER-LOK DISPOSABLE SYRINGE WITH BD LUER-LOK TIP

MDR report key: 10659673 · Received October 9, 2020

Report

Report Number
9614033-2020-00139
Event Type
Malfunction
Date Received
October 9, 2020
Date of Event
September 4, 2020
Report Date
November 9, 2020
Manufacturer
BECTON DICKINSON DE MEXICO
Product Code
FMF
UDI-DI
30382903096573
PMA / PMN Number
K151766
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

H.6. INVESTIGATION: ONE SAMPLE RECEIVED FOR INVESTIGATION, VISUAL INSPECTION AND LEAKAGE TEST WAS PERFORMED, NO DEFECTS FOUND. FURTHERMORE, A DEVICE HISTORY RECORD REVIEW SHOWED NO REJECTED INSPECTIONS OR QUALITY ISSUES DURING THE PRODUCTION OF THE PROVIDED LOT NUMBER THAT COULD HAVE CONTRIBUTED TO THE REPORTED DEFECT. CAPA#1132752 WAS INITIATED.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD LUER-LOK¿ DISPOSABLE SYRINGE WITH BD LUER-LOK¿ TIP LEAKED BEFORE USE. THIS COMPLAINT WAS CREATED TO CAPTURE THE 1ST OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CALLER REPORTED NEEDLE IS SYRINGE IS LEAKING."

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. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE BD LUER-LOK¿ DISPOSABLE SYRINGE WITH BD LUER-LOK¿ TIP LEAKED BEFORE USE. THIS COMPLAINT WAS CREATED TO CAPTURE THE 1ST OF 2 RELATED INCIDENTS. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: "CALLER REPORTED NEEDLE IS SYRINGE IS LEAKING."

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1123938 BD LUER-LOK DISPOSABLE SYRINGE WITH BD LUER-LOK TIP PISTON SYRINGE FMF BECTON DICKINSON DE MEXICO 309657 0044630 30382903096573

Patients

Seq Age Sex Outcome Treatment
1 11 YR Other