Bard recalls POWERPORT ClearVUE implantable ports with incorrect patient ID card flushing instructions. This may lead to improper catheter care. 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 that came with incorrect flushing instructions on the patient ID card. This could lead to improper catheter care if users follow the wrong instructions.
The patient ID card included with the port has incorrect instructions for flushing the catheter. If users follow the wrong instructions, it could lead to improper catheter care. However, the hazard does not involve immediate physical harm or serious injury.
Patients with Bard POWERPORT ClearVUE implantable ports who received the recalled model with incorrect flushing instructions are affected. Those with the specific lot numbers and reference codes listed in the recall are most at risk.
Check if your POWERPORT ClearVUE port has the reference number REF 5668362 and the specific lot numbers listed in the UDI codes (e.g., REAN0059, REAN1125, etc.).
Verify the flushing instructions on the patient ID card match the correct procedure for Bard POWERPORT ClearVUE ports.
The patient ID card included with the port has incorrect flushing instructions, which could lead to improper catheter care.
No, but you should check the flushing instructions on the patient ID card to ensure they are correct.
Check the patient ID card for correct flushing instructions. If the instructions are incorrect, contact Bard for further guidance.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1767-2018 — Bard Bard Hello, I own a Bard that is covered by recall Z-1767-2018 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.
