Bard recalls GlidePath long-term hemodialysis catheters with preloaded stylet (model 5397270) due to tunneler 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 5397270) because the tunneler tip may break during catheter placement. This could lead to complications if the catheter becomes dislodged or damaged.
The molded tip of the tunneler can break during catheter placement, which may cause the catheter to become dislodged or damaged. This could lead to complications such as infection or improper function.
Hemodialysis patients and healthcare providers using the recalled catheters. Those with the specific model and lot numbers are most at risk.
Check for the model number 5397270, 14.5F, straight, 27cm length. The catheter has lot numbers REDN1397 (exp. 3/31/2020), RECX2707 (exp. 7/31/2020), RECX1119 (exp. 3/31/2020), and RECU2783 (exp. 1/31/2020).
Verify the model number (5397270), size (14.5F), and length (27cm) to confirm if your catheter is affected.
Reach out to your healthcare provider to discuss potential risks and next steps for the recalled catheter.
The molded tip of the tunneler may break during catheter placement, potentially causing dislodgement or damage.
Check the model and lot numbers to confirm if it's affected. Contact your healthcare provider for guidance.
The recall is due to a potential risk of the tunneler tip breaking during placement, which could lead to complications if the catheter becomes dislodged.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2392-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2392-2019 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.
