Bard recalls EQUISTREAM XK Long-Term Hemodialysis Catheters with preloaded stylet (REF 5913270) due to tunneler tip breaking during placement, potentially causing complications. Affected units sold between 2020-09-30 and 2020-07-31.
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 specific hemodialysis catheters because the tunneler tip may break during placement. This could lead to complications like infections or improper catheter function. Patients using these catheters should contact Bard immediately for guidance.
The tunneler tip can break during catheter placement, which may cause the catheter to become dislodged or improperly positioned. This could lead to complications such as infection or ineffective dialysis treatment.
Patients using the recalled EQUISTREAM XK hemodialysis catheters (model 5913270) are most at risk. Healthcare providers who have placed these catheters may also need to check their equipment.
Check for the product code 5913270 on the catheter packaging or label. The catheter has a 16F size, straight configuration, and 27cm length. It was sold between September 30, 2020, and July 31, 2020.
Reach out to Bard's customer service for specific instructions on how to handle the recalled catheter.
The tunneler tip may break during catheter placement, which could cause complications like infection or improper function.
The affected model is 5913270 (EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet).
Check for the product code 5913270 on the catheter packaging or label. The catheter has a 16F size, straight configuration, and 27cm length.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2379-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2379-2019 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.
