Bard recalls GlidePath long-term hemodialysis catheters with preloaded stylet (model 5393270) 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 5393270) 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 are affected. Patients with the specific model and lot numbers are most at risk.
Check for the model number 5393270, 14.5F, straight, 27cm length. The catheter has specific lot numbers and expiration dates listed in the product description.
Review the product description for the model number 5393270, 14.5F, straight, 27cm length and associated lot numbers.
The recall is due to complaints about the tunneler tip breaking or being damaged during catheter placement, which could cause complications.
Check the product details for the model number and lot numbers to see if it is affected. Contact Bard for further instructions.
Yes, the affected units have 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-2385-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2385-2019 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.
