Smiths Medical recalls ProPort Low Profile Plastic Venous Access Systems with a risk of plastic port housing and reservoir separating due to manufacturing defect. Affected units have specific lot numbers and UDI/DI codes.
The plastic port housing and port reservoir of the ProPort Plastic Implantable Ports may separate because of a manufacturing defect.
Smiths Medical is recalling certain ProPort Low Profile Plastic Venous Access Systems because the plastic port housing and reservoir may separate due to a manufacturing defect. This could lead to the catheter becoming unsafe to use.
The plastic port housing and reservoir may separate because of a manufacturing defect. This separation could cause the catheter to become unsafe to use, potentially leading to complications for patients.
Patients and healthcare providers using the recalled ProPort Low Profile Plastic Venous Access Systems are most at risk. The specific units affected are those with the listed lot numbers and UDI/DI codes.
Check for the lot numbers listed in the recall: 3916028, 3969277, 4006477, and other specific numbers. Also look for the UDI/DI code 10610586012778 on the product.
Look for the lot numbers and UDI/DI code on the product to confirm if it is affected.
The plastic port housing and reservoir may separate due to a manufacturing defect, which could make the catheter unsafe to use.
Check the product for the listed lot numbers and UDI/DI code to see if it is affected. If it is, contact Smiths Medical for further instructions.
Affected products have specific lot numbers: 3916028, 3969277, 4006477, and other numbers listed in the recall. Also check for the UDI/DI code 10610586012778.
We’ve drafted a message you can send Smiths Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-1287-2025 — Smiths Medical Smiths Medical Hello, I own a Smiths Medical that is covered by recall Z-1287-2025 from Smiths Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
