PlainRecalls
FDA Devices Critical Class I Ongoing

smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems, 82-24

Reported: March 26, 2025 Initiated: February 13, 2025 #Z-1286-2025

Product Description

smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems, 82-24

Reason for Recall

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

Details

Recalling Firm
Smiths Medical ASD, Inc.
Units Affected
0 units
Distribution
Worldwide distribution.
Location
Minneapolis, MN

Frequently Asked Questions

What product was recalled?
smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems, 82-24. Recalled by Smiths Medical ASD, Inc.. Units affected: 0 units.
Why was this product recalled?
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Which agency issued this recall?
This recall was issued by the FDA Devices on March 26, 2025. Severity: Critical. Recall number: Z-1286-2025.