FDA Adverse Event Malfunction Summary report: N

13 MM SS VIAL ACCESS DEVICE

MDR report key: 20881423 · Received December 9, 2024

Report

Report Number
9616066-2024-01971
Event Type
Malfunction
Date Received
December 9, 2024
Date of Event
October 10, 2024
Report Date
January 5, 2025
Manufacturer
BECTON DICKINSON
Product Code
LHI
UDI-DI
07613203011792
PMA / PMN Number
K233021
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NE, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

DUE TO NO SAMPLE BEING RECEIVED, AN INVESTIGATION COULD NOT BE PERFORMED, AND A ROOT CAUSE COULD NOT BE DETERMINED. NO PRODUCT WILL BE RETURNED PER CUSTOMER. NO INVESTIGATION WAS PERFORMED.

Additional Manufacturer Narrative · 0

INITIAL MDR SUBMISSION. A FOLLOW UP MDR WILL BE SUBMITTED IF ADDITIONAL INFORMATION, A DEVICE EVALUATION, OR A DEVICE HISTORY REVIEW IS COMPLETED.

Description of Event or Problem · 0

MATERIAL#: 2203E. BATCH NUMBER#: 23125149. IT WAS REPORTED BY CUSTOMER THAT LEAKING FROM ANYWHERE BUT DISPENSING POINT - DURING USE. RCC RECEIVED A COMPLAINT VIA EMAIL. COVE ID COMPLAINT (B)(4). DATE OF COMPANY AWARENESS 10/10/2024. MERCK FG BATCH # Y008133. BD VIAL ADAPTER BATCH 23125149. PQC CATEGORY. LEAKING FROM ANYWHERE BUT DISPENSING POINT - DURING USE.

Description of Event or Problem · 0

MATERIAL#: 2203E BATCH NUMBER#: 23125149 IT WAS REPORTED BY CUSTOMER THAT LEAKING FROM ANYWHERE BUT DISPENSING POINT - DURING USE VERBATIM#: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. COVE ID COMPLAINT-(B)(4) DATE OF COMPANY AWARENESS 10/10/2024 MERCK FG BATCH # Y008133 BD VIAL ADAPTER BATCH 23125149 PQC CATEGORY LEAKING FROM ANYWHERE BUT DISPENSING POINT - DURING USE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1710756 13 MM SS VIAL ACCESS DEVICE SET, I.V. FLUID TRANSFER LHI BECTON DICKINSON 23125149 07613203011792

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown