Bard recalls POWERPORT ClearVUE implantable ports with incorrect flushing instructions that could lead to improper use. Affected units have specific lot numbers and reference codes.
The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port with Smooth Septum contains incorrect port flushing instructions.
Bard is recalling POWERPORT ClearVUE implantable ports with a smooth septum that have incorrect port flushing instructions in the patient ID card. This could lead to improper use if the instructions are followed incorrectly.
The patient ID card contains incorrect port flushing instructions, which could lead to improper use of the port. If the instructions are followed incorrectly, it might cause complications during medical procedures.
Patients with Bard POWERPORT ClearVUE implantable ports who received the recalled model are affected. Those with the specific lot numbers and reference codes listed in the recall are most at risk.
Check the patient ID card for the product name 'POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter'. The specific lot numbers and reference codes are listed in the recall notice.
Review the patient ID card for the product name and ensure it matches the recalled model.
The recalled model is POWERPORT ClearVUE isp with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter, REF 5666362.
Check the patient ID card for the product name and look for the specific lot numbers and reference codes listed in the recall notice.
Review the patient ID card for the product name and ensure it matches the recalled model. Contact Bard for further instructions.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1766-2018 — Bard Bard Hello, I own a Bard that is covered by recall Z-1766-2018 from Bard. 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.
