Bard recalls GlidePath long-term hemodialysis catheters with preloaded stylet (model 5393420) due to tunneler tip breaking during 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 certain GlidePath hemodialysis catheters because the tunneler tip may break during catheter placement. This could lead to complications for patients needing dialysis treatment.
The tunneler tip can break during catheter placement, which may cause complications such as infection or improper catheter function. This is a risk during the procedure but not during normal use.
Patients receiving hemodialysis treatment and healthcare providers who use these catheters are affected. Those with the specific model and lot numbers are most at risk.
Check for the model number 5393420, 14.5F, straight, 42cm length. Affected units have lot numbers RECZ2997 (exp. 8/31/2020), RECX0854 (exp. 3/31/2020), RECW0386 (exp. 7/31/2020), or RECX1190 (exp. 1/31/2020).
Verify the model number, size, and lot numbers listed in the recall notice to confirm if your catheter is affected.
The tunneler tip may break during catheter placement, which could lead to complications for patients needing dialysis treatment.
Check for the model number 5393420, 14.5F, straight, 42cm length with lot numbers RECZ2997 (exp. 8/31/2020), RECX0854 (exp. 3/31/2020), RECW0386 (exp. 7/31/2020), or RECX1190 (exp. 1/31/2020).
The recall notice does not specify a remedy, so contact Bard directly for guidance on 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-2386-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2386-2019 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.
