FDA Enforcement Class II Ongoing

smiths medical portex, 15mm Double Swivel Connector: a) REF 100/255/150; b) REF 100/255/150JP; c) REF 100/255/150 JS

Recall: Z-0144-2025 · Reported October 30, 2024

Enforcement

Recall Number
Z-0144-2025
Event ID
95181
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Smiths Medical ASD Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
October 30, 2024
Initiation Date
July 18, 2024
Classification Date
October 23, 2024
Address
6000 Nathan Ln N, N/A, Minneapolis, MN, 55442-1690, United States

Description

smiths medical portex, 15mm Double Swivel Connector: a) REF 100/255/150; b) REF 100/255/150JP; c) REF 100/255/150 JS

Reason

Uncertainty in the seal integrity of the sterile packaging.

Code Info

a) REF 100/255/150, UDI/DI 35019315022399, Lot Numbers: 4125006; UDI/DI 35019315010990, Lot Numbers: 4159808, 4161750; UDI/DI 35019315011003, Lot Numbers: 4131840; UDI/DI 35019315018156, Lot Numbers: 4131559; UDI/DI 35019315022405, Lot Numbers: 4122011, 4127688; b) REF 100/255/150JP, UDI/DI 35019315010990, Lot Numbers: 4089148, 4107293, 4122008, 4147817, 4138707, 4159808; c) REF 100/255/150 JS, UDI/DI 35019315010990, Lot Numbers: 4122008, 4147817, 4159808

Distribution

Worldwide distribution.

Quantity

34,141 units