FDA Adverse Event Malfunction Summary report: N

BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLE

MDR report key: 20147718 · Received September 5, 2024

Report

Report Number
9617032-2024-01409
Event Type
Malfunction
Date Received
September 5, 2024
Date of Event
August 8, 2024
Report Date
August 12, 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
FR
Reporter Occupation
NURSE
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

B3. DATE OF EVENT IS UNKNOWN. THE DATE RECEIVED BY MANUFACTURER HAS BEEN USED FOR THIS FIELD. INVESTIGATION SUMMARY: "MATERIAL #: 360210. LOT/BATCH #: 4003277. BD HAD NOT RECEIVED SAMPLES OR PHOTOS FOR INVESTIGATION. THEREFORE, 10 RETENTION SAMPLES FROM BD INVENTORY WERE EVALUATED BY FUNCTIONAL DRAW TESTING AND NO ISSUES WERE OBSERVED RELATING TO CLOG AS ALL SAMPLES MET SPECIFICATIONS. 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 CLOG. 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 BD VACUTAINER® PRECISIONGLIDE¿ MULTIPLE SAMPLE NEEDLES, THE CANNULAS WERE CLOGGED PREVENTING BLOOD SAMPLE COLLECTION. THIS OCCURRED WITH AN UNSPECIFIED NUMBER OF DEVICES. THERE WAS NO REPORT OF ADVERSE IMPACT TO PATIENTS OR USERS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1835380 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