FDA Adverse Event Malfunction Summary report: N

BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE

MDR report key: 8280504 · Received January 28, 2019

Report

Report Number
9616656-2019-00112
Event Type
Malfunction
Date Received
January 28, 2019
Date of Event
January 7, 2019
Report Date
February 12, 2019
Manufacturer
BECTON DICKINSON AND CO.
Product Code
FMI
UDI-DI
00382903251056
PMA / PMN Number
K131358
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION: ONE SEALED 31G X 8MM PEN NEEDLE SAMPLE WAS RETURNED FROM LOT. NO. 8122822, CAT. NO. 325105. VISUAL EXAMINATION WAS CARRIED OUT ON THE RETURNED SAMPLE AND A CANNULA THROUGH SHIELD AND COVER WAS OBSERVED. A LOT HISTORY REVIEW WAS CARRIED OUT AND NO RELATED NON CONFORMANCES WERE RAISED IN ASSOCIATION WITH THIS PACKAGED LOT CONCLUDING ALL INSPECTIONS WERE PERFORMED PER THE APPLICABLE OPERATIONS AND MET QC SPECIFICATIONS. ROOT CAUSE OF THIS ISSUE WAS INCORRECT LOADING OF THE SHIELD TO THE HUB AT THE SHIELDING STATION.

Description of Event or Problem · 0

IT WAS REPORTED THAT BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE WENT THROUGH OUTER SHIELD AND HAD STERILITY ISSUES. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.

Additional Manufacturer Narrative · 1

A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS ANTICIPATED, BUT IS NOT COMPLETE. UPON COMPLETION, A SUPPLEMENTAL REPORT WILL BE FILED.

Description of Event or Problem · 1

IT WAS REPORTED THAT BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE WENT THROUGH OUTER SHIELD AND HAD STERILITY ISSUES. NO SERIOUS INJURY OR MEDICAL INTERVENTION WAS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
76133 BD MICRO-FINE ULTRA¿ INSULIN PEN NEEDLE PEN NEEDLE FMI BECTON DICKINSON AND CO. 8122822 00382903251056

Patients

Seq Age Sex Outcome Treatment
1 Other