Bard recalls EQUISTREAM XK Long-Term Hemodialysis Catheters with preloaded stylet (REF 5913190) 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 long-term hemodialysis catheters because the tunneler tip can break during placement. This breakage may cause complications for patients needing dialysis treatment.
The tunneler tip can break during catheter placement, which may lead to complications like infection or improper catheter function. This breakage happens during the procedure, not after the catheter is in place.
Patients using hemodialysis treatments with this specific catheter model are most at risk. Healthcare providers who place the catheter may also be affected if they use the recalled units.
Check for the product code 5913190 on the catheter label. The catheter has a specific length (19cm), 16F size, and straight configuration. Lot numbers include RECZ2628 (exp. 9/30/2020), RECX3045 (exp. 7/31/2020), and RECW1365 (exp. 4/30/2020).
Look for the product code 5913190, 16F size, straight configuration, and 19cm length on the catheter label.
The tunneler tip can break during catheter placement, which may cause complications for patients needing dialysis treatment.
Check for the product code 5913190, 16F size, straight configuration, and 19cm length. Lot numbers include RECZ2628 (exp. 9/30/2020), RECX3045 (exp. 7/31/2020), and RECW1365 (exp. 4/30/2020).
The recall record does not specify a remedy, so contact Bard directly for guidance.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2377-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2377-2019 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.
