Bard recalls POWERPORT ClearVUE Implantable Ports with incorrect flushing instructions that could lead to improper patient care. Affected units have specific lot numbers and identifiers.
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 patient care if the instructions are followed incorrectly.
The Patient ID Card includes incorrect port flushing instructions. If healthcare providers follow these instructions, it could lead to improper patient care. This is a documentation error, not a physical defect in the port.
Patients with Bard POWERPORT ClearVUE Implantable Ports may be affected. Healthcare providers who use these ports are most at risk of administering incorrect care.
Check for the POWERPORT ClearVUE Implantable Port with Smooth Septum, 6F ChronoFlex, Polyurethane Catheter. The lot numbers include specific UDI codes like REAN0063, REAN1123, REAP0467, REAY1733, REBS1266, REBV1731, REBX1626, and REBY0777.
Review the flushing instructions on the Patient ID Card to ensure they are correct for your specific port model.
The Patient ID Card contains incorrect port flushing instructions that could lead to improper patient care if followed.
Check the Patient ID Card for correct flushing instructions. If unsure, contact Bard for guidance.
Look for the specific lot numbers in the UDI codes: REAN0063, REAN1123, REAP0467, REAY1733, REBS1266, REBV1731, REBX1626, or REBY0777.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1760-2018 — Bard Bard Hello, I own a Bard that is covered by recall Z-1760-2018 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.
