Bard recalls POWERPORT ClearVUE Slim catheters with incorrect port flushing instructions on the Patient ID Card. This could lead to improper catheter care. Affected units have specific lot numbers and serial 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 Slim catheters because the Patient ID Card includes incorrect port flushing instructions. This could lead to improper catheter care if users follow the wrong instructions.
The Patient ID Card has incorrect port flushing instructions, which could lead to improper catheter care if users follow the wrong steps. This might cause complications like infection or blockage if the catheter isn't flushed correctly.
Patients using Bard POWERPORT ClearVUE Slim catheters with the specific lot numbers listed in the recall. Healthcare providers who administer these catheters are most at risk.
Check for the specific lot numbers and serial codes listed in the recall notice. These are unique identifiers for the affected POWERPORT ClearVUE Slim catheters.
Review the port flushing instructions on the Patient ID Card to ensure they match the correct procedure for the POWERPORT ClearVUE Slim catheter.
The Patient ID Card contains incorrect port flushing instructions, which could lead to improper catheter care if users follow the wrong steps.
Check the Patient ID Card for the correct port flushing instructions. If the instructions are incorrect, contact Bard for guidance.
Look for the specific lot numbers and serial codes listed in the recall notice, which include unique identifiers like REAN0061, REAP0772, etc.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-1771-2018 — Bard Bard Hello, I own a Bard that is covered by recall Z-1771-2018 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.
