FDA Adverse Event Malfunction Summary report: N

VETRIJEC

MDR report key: 23707561 · Received December 3, 2025

Report

Report Number
1000138447-2025-00002
Event Type
Malfunction
Date Received
December 3, 2025
Date of Event
November 4, 2025
Report Date
November 7, 2025
Manufacturer
HLB LIFE SCIENCE CO LTD
Product Code
FMF
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AR, US
Reporter Occupation
501

Narratives

Description of Event or Problem · 0

(B)(6) SAID "ABOUT THE SPECIFIC ISSUE, I CAN SPEAK ABOUT MY OWN EXPERIENCE AS WELL AS A COUPLE OF MY FELLOW TECHNICIANS HAD REGARDING THE SYRINGES. THE METHOD I USE WHEN UNWRAPPING THEM IS I OPEN ALL THE SYRINGES AND PUT THEM INTO THE CARDBOARD BOX, BUT MANY OF THE PLASTIC CAPS WERE COMING OFF OF THE NEEDLES. I NOTICED THIS WHEN I REACHED IN TO GRAB A HANDFUL OF THEM AND WAS STUCK BY A FEW "HOT" NEEDLES. I IMMEDIATELY PUT A WARNING ON THE BOX FOR OTHER TECHS TO SEE AND TO USE CAUTION. BUT WITHIN A FEW HOURS, ANOTHER TECH WAS OPENING EACH SYRINGE ONE AT A TIME AND THE CAPS WERE FALLING OFF WITHOUT MUCH DISTURBANCE, AND SHE WAS ALSO STUCK A COUPLE OF TIMES. NOTHING SEVERE. I WOULD NORMALLY IGNORE THIS BUT BECAUSE I HAD JUST PURCHASED SUCH A LARGE QUANTITY OF THEM, I FIGURED IT WAS WORTH REPORTING. I TRIED TO RECREATE THE SCENARIO AND OPEN A FEW SYRINGES SO THAT YOU CAN HOPEFULLY SEE WHAT I'M TALKING ABOUT. "

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2844598 VETRIJEC 3ML LL WITH 20G X 1", FMF HLB LIFE SCIENCE CO LTD 670235 250723

Patients

Seq Age Sex Outcome Treatment
1 40 YR Female