Bard recalls GlidePath Long-Term Hemodialysis Catheters with preloaded stylet (model 5397500) due to tunneler tip breaking during placement, risking complications.
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 5397500) because the tunneler tip may break during catheter placement. This could lead to complications if the catheter becomes dislodged or damaged.
The tunneler tip may break during catheter placement, which could cause the catheter to become dislodged or damaged. This might lead to complications such as infection or improper function of the dialysis system.
Hemodialysis patients and healthcare providers who use the recalled GlidePath catheters (model 5397500, 14.5F, 50cm) are affected. Patients with existing catheters should check if they have the specific model.
Check for the model number 5397500 on the catheter label. The catheter is 14.5F, straight, 50cm long with a preloaded stylet. It was sold with lot number RECX2780, expiring August 31, 2020.
Look for the model number 5397500 on the catheter label to confirm if it is recalled.
The recall is due to the tunneler tip breaking during placement, which could cause complications if the catheter becomes dislodged or damaged.
Check for the model number 5397500 on the catheter label. The catheter is 14.5F, straight, 50cm long with a preloaded stylet.
The recall does not specify a remedy, so contact Bard directly to discuss next steps.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2395-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2395-2019 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.
