FDA Enforcement Class I Ongoing

smiths medical ProPort Plastic Venous Access System, PolyFlow Catheter, 2.6 (7.8Fr) O.D. x 1.6mm I.D., 8.5Fr Introducer, REF 21-4171-24

Recall: Z-1283-2025 · Reported March 26, 2025

Enforcement

Recall Number
Z-1283-2025
Event ID
96294
Classification
Class I
Status
Ongoing
Product Type
Devices
Firm
Smiths Medical ASD, Inc.
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
March 26, 2025
Initiation Date
February 13, 2025
Classification Date
March 18, 2025
Address
6000 Nathan Ln N, N/A, Minneapolis, MN, 55442-1690, United States

Description

smiths medical ProPort Plastic Venous Access System, PolyFlow Catheter, 2.6 (7.8Fr) O.D. x 1.6mm I.D., 8.5Fr Introducer, REF 21-4171-24

Reason

The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.

Code Info

UDI/DI 10610586012716, Lot Numbers: 3941279, 3969275, 3984421, 4022601, 4136364, 4148590, 4153873, 4196768, 4227788, 4232310, 4235600, 4248718, 4276227, 4302980, 4307478, 4317093, 4325880, 4358053, 4358054, 4395512, 4415445, 4420760, 4437255, 4449234, 4449877, 4460620, 6013083, 6003891, 6053532, 6062026.

Distribution

Worldwide distribution.

Quantity

1961 units