FDA Adverse Event Malfunction Summary report: N

13 MM SS VIAL ACCESS DEVICE

MDR report key: 20883610 · Received December 9, 2024

Report

Report Number
9616066-2024-01973
Event Type
Malfunction
Date Received
December 9, 2024
Date of Event
October 17, 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#: 23105217. IT WAS REPORTED BY CUSTOMER THAT VIAL ADAPTOR LEAKING DURING USE VERBATIM#: RCC RECEIVED A COMPLAINT VIA EMAIL. COVE ID - (B)(4). DATE OF COMPANY AWARENESS- 17-OCT-24. MERCK FG BATCH # - Y008793. BD VIAL ADAPTER BATCH - 23105217. PQC CATEGORY - VIAL ADAPTOR LEAKING DURING USE.

Description of Event or Problem · 0

MATERIAL#: 2203E. BATCH NUMBER#: 23105217. IT WAS REPORTED BY CUSTOMER THAT VIAL ADAPTOR LEAKING DURING USE. VERBATIM#: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. COVE ID - (B)(4). DATE OF COMPANY AWARENESS- 17-OCT-2024. MERCK FG BATCH # - Y008793. BD VIAL ADAPTER BATCH - 23105217. PQC CATEGORY - VIAL ADAPTOR LEAKING DURING USE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2477100 13 MM SS VIAL ACCESS DEVICE SET, I.V. FLUID TRANSFER LHI BECTON DICKINSON 23105217 07613203011792

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown