Bard recalls GlidePath Long-Term Hemodialysis Catheters with Preloaded Stylet (REF 5393230) due to molded tip breaking during placement, potentially causing complications. Affected units have specific lot numbers and expiration dates.
The action is being initiated due to complaints received concerning the molded tip of the tunneler breaking or is damaged during the placement procedure of the catheter.
Bard is recalling GlidePath Long-Term Hemodialysis Catheters with Preloaded Stylet (model 5393230) because the molded tip can break during catheter placement. This breakage may lead to complications like infection or dislodgement, which could harm patients receiving dialysis.
The molded tip of the tunneler can break or become damaged during catheter placement. This breakage may cause the catheter to dislodge or become infected, leading to serious complications for patients needing dialysis.
Patients using hemodialysis treatments with this specific catheter model are most at risk. Healthcare providers who place the catheter during dialysis procedures may also be affected.
Check for the model number 5393230 on the catheter packaging or label. Affected units have specific lot numbers and expiration dates listed in the recall notice.
Review the catheter's model number and lot numbers to confirm if it matches the recalled items.
The molded tip of the tunneler can break or become damaged during catheter placement, potentially causing complications like infection or dislodgement.
Check the model number and lot numbers to confirm if it's affected; the recall notice does not specify a remedy for affected units.
Yes, a broken tip could lead to catheter dislodgement or infection, which may cause serious complications for patients receiving dialysis.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2384-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2384-2019 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
