Bard recalls EQUISTREAM XK Long-Term Hemodialysis Catheters with preloaded stylet (REF 5913310) due to tunneler tip breaking during placement, potentially causing complications.
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 that may have a broken tunneler tip during placement. This could lead to complications if the catheter is used without proper fixation.
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 bleeding if the catheter is not securely anchored.
Hemodialysis patients using the recalled catheters (model 5913310, 16F, 31cm) are most at risk. Healthcare providers who placed these catheters should check for tip damage.
Check for the product code 5913310, 16F size, 31cm length, and lot number RECX3001 (expiring 9/30/2020) on the catheter packaging or label.
Inspect the tunneler tip for cracks or breaks before use. If damaged, do not use the catheter.
Reach out to your healthcare provider to determine if the catheter needs replacement or repair.
Bard recalls these catheters due to complaints about the tunneler tip breaking during placement, which could cause complications.
Look for the product code 5913310, 16F size, 31cm length, and lot number RECX3001 (expiring 9/30/2020) on the catheter.
Do not use the catheter if the tunneler tip is cracked or broken. Contact your healthcare provider for assistance.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-2381-2019 — Bard Bard Hello, I own a Bard that is covered by recall Z-2381-2019 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.
