Bard recalls GlidePath Long-Term Hemodialysis Catheters with preloaded stylet (model 5397230) due to molded tip breaking during catheter placement, risking 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 5397230) because the molded tip can break during catheter placement. This could lead to complications if the catheter becomes dislodged or damaged.
The molded tip of the catheter can break during placement, which may cause the catheter to become dislodged or damaged. This could lead to complications such as infection or improper function of the dialysis system.
Healthcare professionals who use these catheters for hemodialysis treatments are most at risk. Patients receiving dialysis through this specific model may also be affected.
Check for the product code 5397230, 14.5F, straight, 23cm length. Affected units have specific lot numbers and expiration dates listed in the product description.
Review the product code, model, and lot numbers to confirm if your catheter is affected.
The recall indicates the molded tip can break during placement, so it is not safe to use without checking if it's affected.
Check the product code and lot numbers to see if it's affected; if so, contact Bard for guidance.
Look for the product code 5397230, 14.5F, straight, 23cm length with specific lot numbers and expiration dates listed in the product description.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2391-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2391-2019 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.
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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.
