FDA Adverse Event Malfunction Summary report: N

BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLE

MDR report key: 20263903 · Received September 19, 2024

Report

Report Number
9617032-2024-01489
Event Type
Malfunction
Date Received
September 19, 2024
Date of Event
August 21, 2024
Report Date
August 23, 2024
Manufacturer
BECTON, DICKINSON AND COMPANY (BD)
Product Code
FMI
UDI-DI
30382903602101
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NZ
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION SUMMARY: "MATERIAL #: 360210. LOT/BATCH #: 4003277. BD RECEIVED 30 SAMPLES FOR INVESTIGATION. TEN (10) OF THE SAMPLES WERE EVALUATED BY FUNCTIONAL DRAW TESTING AND THE INDICATED FAILURE MODE FOR CLOGGED CANNULA WITH THE INCIDENT LOT WAS NOT OBSERVED AS ALL PRODUCT SPECIFICATIONS WERE MET. BASED ON A REVIEW OF THE DEVICE HISTORY RECORD FOR THE INCIDENT LOT, ALL PRODUCT SPECIFICATIONS AND REQUIREMENTS FOR LOT RELEASE WERE MET. THERE WERE NO RELATED QUALITY ISSUES DURING MANUFACTURING OF THE PRODUCT. THIS COMPLAINT IS UNABLE TO BE CONFIRMED FOR THE INDICATED FAILURE MODE CLOGGED CANNULA. BD WAS NOT ABLE TO IDENTIFY A ROOT CAUSE FOR THE INDICATED FAILURE MODE. COMPLAINTS RECEIVED FOR THIS DEVICE AND REPORTED CONDITION WILL CONTINUE TO BE TRACKED AND TRENDED. OUR BUSINESS TEAM REGULARLY REVIEWS THE COLLECTED DATA FOR IDENTIFICATION OF EMERGING TRENDS."

Description of Event or Problem · 0

IT WAS REPORTED WHILE USING AN UNSPECIFIED NUMBER OF BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLES, THE DEVICES WERE CLOGGED, NOT ALLOWING FLUID TO PASS. THERE WAS NO REPORT OF ADVERSE IMPACT TO PATIENTS OR USERS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
226783 BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLE BLOOD COLLECTION NEEDLE FMI BECTON, DICKINSON AND COMPANY (BD) 4003277 30382903602101

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown