RecallCheckr

Critical recall: Death or serious injury has been reported or is considered likely. Stop using this product now.

Smiths Medical ASD, Inc. 2025-03-26 Health critical FDA
Health · FDA · Recall #FDA-Z-1286-2025

smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems,… Recall

Issued March 26, 2025 · Smiths Medical ASD, Inc.

In March 2025, Smiths Medical ASD, Inc. recalled the smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems,…, a critical health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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

What you should do

  1. 1 Stop using smiths medical ProPort Plastic Venous Access System, Implantable Venous Access Systems,… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Smiths Medical ASD, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Smiths Medical ASD, Inc.
Category
Health
Recall date
March 26, 2025
Units affected
Not reported
Sold at
Worldwide distribution.
Recall number
FDA-Z-1286-2025
Made in
United States
Issuing agency
FDA

In context

  • Smiths Medical ASD, Inc. has 3 recalls in our database, including 2 rated Critical.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 691st Health recall we've logged in 2025.
Read the official FDA notice

Related recalls