Bard recalls GlidePath long-term hemodialysis catheters with broken tunneler tips that may cause complications during placement. Affected models include REF/Product code:5396240, 14.5F, Alphacurve, 19cm length. Contact Bard for details.
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 long-term hemodialysis catheters because the tunneler tip can break during catheter placement. This breakage may lead to complications for patients needing dialysis treatment.
The tunneler tip can break during catheter placement, potentially causing complications like infection or dislodgement. This breakage occurs during the procedure, not after the catheter is in place.
Patients using hemodialysis treatment with the recalled catheters are most at risk. Healthcare providers who place these catheters may also be affected.
Check for the product code 5396240, 14.5F size, Alphacurve design, and 19cm length. The catheter has a unique identifier (UDI) starting with 00801741012259 and specific lot numbers.
Look for the product code 5396240, 14.5F, Alphacurve, 19cm length, and UDI starting with 00801741012259.
The tunneler tip can break during catheter placement, potentially causing complications for patients needing dialysis.
The recall record does not specify a remedy, so contact Bard directly for guidance.
Yes, the catheter has lot numbers RECZ1119 (exp. 8/31/2020), RECX2706 (exp. 7/31/2020), RECX1189 (exp. 8/31/2020), and RECX0986 (exp. 8/31/2020).
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2388-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2388-2019 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.
