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Smiths Medical ASD, Inc. recalls smiths medical ProPort Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm (7.8Fr) O.
Recalled March 26, 2025 · FDA recall Z-1282-2025 · Smiths Medical ASD
Hazard
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect. · FDA Class I
Units
1695 units
Sold at
Worldwide distribution.
Description
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Product
smiths medical ProPort Plastic Venous Access System, Pre-assembled with PolyFlow Polyurethane Catheter, 2.6mm (7.8Fr) O.D. x 1.6mm I.D., 8.6Fr Introducer, REF 21-4165-24
Manufacturer(s)
Smiths Medical ASD, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →