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Smiths Medical ASD, Inc. recalls smiths medical ProPort Plastic Venous Access System, PolyFlow Polyurethane Catheter, 1.9mm O.D. (5.8 Fr) x 1.0mm I.D., R
Recalled March 26, 2025 · FDA recall Z-1279-2025 · 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
2311 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, PolyFlow Polyurethane Catheter, 1.9mm O.D. (5.8 Fr) x 1.0mm I.D., REF 21-4152-24
Manufacturer(s)
Smiths Medical ASD, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →