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Recall Observatory FDA recall evidence

Device product

smiths medical ProPort Plastic Venous Access System, Silicone Catheter, 2.8mm (8.4Fr) O.D. x 1.0mm I.D., 9 Fr Introducer, REF 21-4151-24

Z-1278-2025

February 13, 2025

Class I

Product summary

Firm
Smiths Medical ASD, Inc.
Event
Event 96294
Status
Ongoing
Classification
Class I
Quantity
643 units
Official record key
device-enforcement:Z-1278-2025

Official wording

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

Code information: UDI/DI 10610586012532, Lot Numbers: 3968088, 4052396, 4063411, 4101698, 4122782, 4219344, 4232319, 4235596, 4242786, 4317072, 4325879, 4397749, 4420759, 4445594, 4449874.

Distribution pattern: Worldwide distribution.

Derived failure modes

  • Manufacturing or process control

    reason.manufacturing_process_control · v1.0.0

    manufacturing defect