FDA Adverse Event Malfunction Summary report: N

BD ECLIPSE¿ NEEDLE

MDR report key: 7190867 · Received January 15, 2018

Report

Report Number
8041187-2017-00294
Event Type
Malfunction
Date Received
January 15, 2018
Date of Event
December 22, 2017
Report Date
April 3, 2018
Manufacturer
BECTON DICKINSON MEDICAL (SINGAPORE)
Product Code
FMI
UDI-DI
30382903057611
PMA / PMN Number
K161170
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

CAPAS (B)(4) WERE OPENED TO IDENTIFY AND ADDRESS THE POTENTIAL CAUSES OF SAFETY SHIELD DISENGAGEMENT. ADDITIONALLY, FIELD ACTION NOTIFICATION MSS-16-837-FA WAS INITIATED AND A PRODUCT ADVISORY LETTER WAS SENT ON 12/29/2016. DATE OF EVENT: UNKNOWN. THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. A DEVICE EVALUATION IS ANTICIPATED, BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 1

INVESTIGATION SUMMARY: SINCE NO SAMPLES DISPLAYING THE CONDITION REPORTED ARE AVAILABLE FOR EXAMINATION, WE WERE UNABLE TO FULLY INVESTIGATE THIS INCIDENT. NO ABNORMALITY AND QN WERE REPORTED ON THE AFFECTED BATCH 6106446 DURING PRODUCTION. INVESTIGATION CONCLUSION: ALTHOUGH THE DEFECT WAS NOT CONFIRMED FOR THIS INSTANCE, BD HAS INVESTIGATED FOLLOWING THE CAPA PROCESS A SIMILAR REPORTED ISSUE AND ACTIONS HAVE BEEN INITIATED.

Additional Manufacturer Narrative · 1

SEVEN REPRESENTATIVE SAMPLES OF BATCH 6106446 WERE RETURNED IN SEALED PACKAGE FOR INVESTIGATION, NO DAMAGE WAS OBSERVED ON THE SAFETY SHIELD. THE SAMPLES WERE SUBJECTED TO SAFETY SHIELD FALL OFF/BREAK OFF TEST, NONE OF THE SAFETY SHIELDS DISENGAGED. THE SAFETY SHIELDS WERE FOUND TO BE INTACT AND PASSED SAFETY SHIELD TEST. HENCE, ROOT CAUSE CANNOT BE DETERMINED.

Description of Event or Problem · 1

IT WAS REPORTED AFTER USE OF THE BD ECLIPSE¿ NEEDLE THE PINK SAFETY SHIELD FALLS OFF. THERE WAS NO REPORT OF INJURY OR MEDICAL INTERVENTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
36091 BD ECLIPSE¿ NEEDLE HYPODERMIC NEEDLE FMI BECTON DICKINSON MEDICAL (SINGAPORE) 6106446 30382903057611

Patients

Seq Age Sex Outcome Treatment
1 Other